Diprion similis isolate iyDipSimi1 chromosome 12, iyDipSimi1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Tenthredinoidea; Diprionidae; Diprioninae; Diprion.
REFSEQ INFORMATION: The reference sequence is identical to\nCM037730.1.\nAssembly name: iyDipSimi1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the United States Department of\nAgriculture on 2021/12/10. The original whole-genome shotgun\nproject has the accession JAJNQI000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: United States Department of Agriculture\nAssembly Date :: 17-NOV-2021\nAssembly Method :: HiFiASM v. 0.16.1-r375; Juicebox Assembly\n Toolkit v. 1.11\nAssembly Name :: iyDipSimi1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 100.0x\nSequencing Technology :: PacBio Sequel; Illumina NovaSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Diprion similis Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Catherine Linnen, University of Kentucky
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
uncharacterized histidine-rich protein DDB_G0274557-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial genome maintenance exonuclease 1-like, transcript variant X4
mitochondrial genome maintenance exonuclease 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitochondrial genome maintenance exonuclease 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mitochondrial genome maintenance exonuclease 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
mitochondrial genome maintenance exonuclease 1-like isoform X1
uncharacterized protein LOC124413328 isoform X2
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase I
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
cold and drought-regulated protein CORA-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
methyl-CpG-binding domain protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
methyl-CpG-binding domain protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
methyl-CpG-binding domain protein 3 isoform X1
methyl-CpG-binding domain protein 3 isoform X2
RNA-binding protein MEX3B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RNA-binding protein MEX3B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein groucho-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein groucho-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
protein groucho-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
protein groucho-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein groucho-like, transcript variant X6
protein groucho-like, transcript variant X5
transducin-like enhancer protein 3-B isoform X5
rab11 family-interacting protein 4, transcript variant X1
rab11 family-interacting protein 4, transcript variant X3
rab11 family-interacting protein 4, transcript variant X2
rab11 family-interacting protein 4, transcript variant X4
rab11 family-interacting protein 4 isoform X1
rab11 family-interacting protein 4 isoform X3
rab11 family-interacting protein 4 isoform X2
rab11 family-interacting protein 4 isoform X4
uncharacterized LOC124413394, transcript variant X1
uncharacterized LOC124413394, transcript variant X2
uncharacterized protein LOC124413394 isoform X1
uncharacterized protein LOC124413394 isoform X2
tubulin polymerization-promoting protein homolog
39S ribosomal protein L52, mitochondrial, transcript variant X1
39S ribosomal protein L52, mitochondrial, transcript variant X2
39S ribosomal protein L52, mitochondrial isoform X1
39S ribosomal protein L52, mitochondrial isoform X2
armadillo repeat-containing protein 8-like, transcript variant X1
armadillo repeat-containing protein 8-like, transcript variant X2
armadillo repeat-containing protein 8-like isoform X1
armadillo repeat-containing protein 8-like isoform X2
islet cell autoantigen 1, transcript variant X2
islet cell autoantigen 1, transcript variant X1
islet cell autoantigen 1, transcript variant X3
hemolymph lipopolysaccharide-binding protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
protein transport protein Sec61 subunit gamma, transcript variant X2
protein transport protein Sec61 subunit gamma, transcript variant X1
protein transport protein Sec61 subunit gamma
NPC intracellular cholesterol transporter 2 homolog a-like
serine/threonine/tyrosine-interacting protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine/tyrosine-interacting protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
serine/threonine/tyrosine-interacting protein-like isoform X1
serine/threonine/tyrosine-interacting protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
tetra-peptide repeat homeobox protein 1-like, transcript variant X2
tetra-peptide repeat homeobox protein 1-like, transcript variant X1
uncharacterized protein LOC124413121 isoform X2
tetra-peptide repeat homeobox protein 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
delta-like protein C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
delta-like protein C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 28% coverage of the annotated genomic feature by RNAseq alignments
disheveled-associated activator of morphogenesis 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
disheveled-associated activator of morphogenesis 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
disheveled-associated activator of morphogenesis 1 isoform X1
disheveled-associated activator of morphogenesis 1 isoform X2
visual system homeobox 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
visual system homeobox 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
visual system homeobox 1-like isoform X2
visual system homeobox 1-like isoform X1
centrosomal protein of 164 kDa-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
centrosomal protein of 164 kDa-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
centrosomal protein of 164 kDa-like, transcript variant X2
centrosomal protein of 164 kDa-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
centrosomal protein of 164 kDa-like isoform X1
centrosomal protein of 164 kDa-like isoform X2
centrosomal protein of 164 kDa-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable cytochrome P450 12a5, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
probable cytochrome P450 12a5, mitochondrial, transcript variant X2
probable cytochrome P450 12a5, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
putative odorant receptor 92a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
putative odorant receptor 92a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
putative odorant receptor 92a isoform X2
putative odorant receptor 92a isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124412969, transcript variant X2
uncharacterized LOC124412969, transcript variant X1
uncharacterized protein LOC124412969 isoform X1
uncharacterized protein LOC124412969 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
acid phosphatase type 7, transcript variant X2
acid phosphatase type 7, transcript variant X1
uncharacterized LOC124413510, transcript variant X1
uncharacterized LOC124413510, transcript variant X2
uncharacterized protein LOC124413510 isoform X1
uncharacterized protein LOC124413510 isoform X2
BTB/POZ domain-containing protein 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
BTB/POZ domain-containing protein 9, transcript variant X1
helix-loop-helix protein delilah-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
helix-loop-helix protein delilah-like isoform X1
helix-loop-helix protein delilah-like, transcript variant X2
helix-loop-helix protein delilah-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
acyl-CoA:lysophosphatidylglycerol acyltransferase 1-like, transcript variant X1
acyl-CoA:lysophosphatidylglycerol acyltransferase 1-like, transcript variant X2
acyl-CoA:lysophosphatidylglycerol acyltransferase 1-like isoform X1
acyl-CoA:lysophosphatidylglycerol acyltransferase 1-like isoform X2
arginase, hepatic, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
arginase, hepatic, transcript variant X2
GPN-loop GTPase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
GPN-loop GTPase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
diphthine--ammonia ligase, transcript variant X2
diphthine--ammonia ligase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
polyadenylate-binding protein-interacting protein 2, transcript variant X3
polyadenylate-binding protein-interacting protein 2, transcript variant X2
polyadenylate-binding protein-interacting protein 2, transcript variant X1
polyadenylate-binding protein-interacting protein 2, transcript variant X4
polyadenylate-binding protein-interacting protein 2, transcript variant X5
polyadenylate-binding protein-interacting protein 2 isoform X3
polyadenylate-binding protein-interacting protein 2 isoform X2
polyadenylate-binding protein-interacting protein 2 isoform X1
polyadenylate-binding protein-interacting protein 2 isoform X4
BCL2/adenovirus E1B 19 kDa protein-interacting protein 3, transcript variant X2
BCL2/adenovirus E1B 19 kDa protein-interacting protein 3, transcript variant X1
BCL2/adenovirus E1B 19 kDa protein-interacting protein 3 isoform X1
BCL2/adenovirus E1B 19 kDa protein-interacting protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
secretory carrier-associated membrane protein 5
N-alpha-acetyltransferase 20, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
TP53-binding protein 1-like, transcript variant X1
TP53-binding protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 68 samples with support for all annotated introns
N-alpha-acetyltransferase 20, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
glutaredoxin-related protein 5, mitochondrial
uncharacterized LOC124413195, transcript variant X1
uncharacterized protein LOC124413195 isoform X1
uncharacterized LOC124413195, transcript variant X2
uncharacterized protein LOC124413195 isoform X2
26S proteasome non-ATPase regulatory subunit 8
nuclear factor related to kappa-B-binding protein-like, transcript variant X3
nuclear factor related to kappa-B-binding protein-like, transcript variant X1
nuclear factor related to kappa-B-binding protein-like, transcript variant X2
nuclear factor related to kappa-B-binding protein-like isoform X1
nuclear factor related to kappa-B-binding protein-like isoform X3
nuclear factor related to kappa-B-binding protein-like isoform X2
60S ribosomal protein L36, transcript variant X1
60S ribosomal protein L36, transcript variant X2
tRNA modification GTPase GTPBP3, mitochondrial, transcript variant X2
tRNA modification GTPase GTPBP3, mitochondrial, transcript variant X1
tRNA modification GTPase GTPBP3, mitochondrial isoform X1
tRNA modification GTPase GTPBP3, mitochondrial isoform X2
vacuolar protein sorting-associated protein 45
cytochrome c oxidase assembly protein COX16 homolog, mitochondrial
centrosome-associated zinc finger protein CP190, transcript variant X1
centrosome-associated zinc finger protein CP190, transcript variant X2
centrosome-associated zinc finger protein CP190
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
tropomyosin Per a 7.0102, transcript variant X10
tropomyosin Per a 7.0102, transcript variant X11
tropomyosin Per a 7.0102, transcript variant X12
tropomyosin Per a 7.0102, transcript variant X17
tropomyosin Per a 7.0102, transcript variant X13
tropomyosin Per a 7.0102, transcript variant X6
tropomyosin Per a 7.0102, transcript variant X5
tropomyosin Per a 7.0102, transcript variant X4
tropomyosin Per a 7.0102, transcript variant X3
tropomyosin Per a 7.0102, transcript variant X8
tropomyosin Per a 7.0102, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
tropomyosin Per a 7.0102, transcript variant X2
tropomyosin Per a 7.0102, transcript variant X1
tropomyosin Per a 7.0102, transcript variant X7
tropomyosin Per a 7.0102, transcript variant X16
tropomyosin Per a 7.0102, transcript variant X15
tropomyosin Per a 7.0102, transcript variant X14
tropomyosin-1, isoforms 9A/A/B isoform X15
tropomyosin-1, isoforms 9A/A/B isoform X16
tropomyosin-1, isoforms 9A/A/B isoform X14
neural cell adhesion molecule 2-like, transcript variant X2
neural cell adhesion molecule 2-like, transcript variant X1
neural cell adhesion molecule 2-like isoform X1
neural cell adhesion molecule 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
neural cell adhesion molecule 1-A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neural cell adhesion molecule 1-A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
neural cell adhesion molecule 1-A-like isoform X1
neural cell adhesion molecule 1-A-like isoform X2
zinc finger protein 845-like, transcript variant X1
zinc finger protein 845-like, transcript variant X2
pyruvate carboxylase, mitochondrial, transcript variant X2
pyruvate carboxylase, mitochondrial, transcript variant X1
pyruvate carboxylase, mitochondrial isoform X2
pyruvate carboxylase, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial, transcript variant X1
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial, transcript variant X2
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial isoform X1
probable methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
echinoderm microtubule-associated protein-like 2, transcript variant X1
echinoderm microtubule-associated protein-like 2, transcript variant X2
echinoderm microtubule-associated protein-like 2 isoform X2
echinoderm microtubule-associated protein-like 2 isoform X1
transfer RNA serine (anticodon CGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
MD-2-related lipid-recognition protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
breast cancer metastasis-suppressor 1-like protein
G-protein coupled receptor moody, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
G-protein coupled receptor moody, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
G-protein coupled receptor moody, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
G-protein coupled receptor moody isoform X1
G-protein coupled receptor moody isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
uncharacterized LOC124413583, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC124413583, transcript variant X2
uncharacterized protein LOC124413583 isoform X1
uncharacterized protein LOC124413583 isoform X2
uncharacterized LOC124412951, transcript variant X1
uncharacterized LOC124412951, transcript variant X2
uncharacterized protein LOC124412951 isoform X2
uncharacterized protein LOC124412951 isoform X1
G patch domain-containing protein 2, transcript variant X4
G patch domain-containing protein 2, transcript variant X3
G patch domain-containing protein 2, transcript variant X1
G patch domain-containing protein 2 isoform X1
G patch domain-containing protein 2, transcript variant X2
G patch domain-containing protein 2 isoform X2
mitochondrial import inner membrane translocase subunit Tim9
mitogen-activated protein kinase kinase kinase 11-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 11-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 11-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 11-like isoform X1
mitogen-activated protein kinase kinase kinase 11-like isoform X2
mitogen-activated protein kinase kinase kinase 11-like isoform X3
mitogen-activated protein kinase kinase kinase 11-like isoform X4
pecanex-like protein 1, transcript variant X1
pecanex-like protein 1, transcript variant X2
thioredoxin, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
thioredoxin, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
thioredoxin, mitochondrial, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
mitochondrial import inner membrane translocase subunit TIM44, transcript variant X2
mitochondrial import inner membrane translocase subunit TIM44, transcript variant X3
mitochondrial import inner membrane translocase subunit TIM44, transcript variant X1
mitochondrial import inner membrane translocase subunit TIM44 isoform X2
mitochondrial import inner membrane translocase subunit TIM44 isoform X1
mitochondrial import inner membrane translocase subunit TIM44, transcript variant X4
mitochondrial import inner membrane translocase subunit TIM44 isoform X3
mitochondrial import inner membrane translocase subunit TIM44 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCCH domain-containing protein 14
ATP-binding cassette sub-family B member 10, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
serine/threonine-protein phosphatase 4 regulatory subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
eukaryotic translation initiation factor 3 subunit F
46 kDa FK506-binding nuclear protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
CLK4-associating serine/arginine rich protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
serine/threonine-protein kinase minibrain
uncharacterized LOC124413283, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
uncharacterized LOC124413283, transcript variant X1
uncharacterized LOC124413282, transcript variant X1
uncharacterized LOC124413282, transcript variant X2
uncharacterized LOC124413147, transcript variant X1
uncharacterized protein LOC124413147 isoform X1
uncharacterized LOC124413147, transcript variant X2
uncharacterized protein LOC124413147 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ribosomal oxygenase 1, transcript variant X1
ribosomal oxygenase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124412939, transcript variant X1
uncharacterized LOC124412939, transcript variant X2
uncharacterized protein LOC124412939 isoform X2
uncharacterized protein LOC124412939 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
tetratricopeptide repeat protein 27, transcript variant X2
tetratricopeptide repeat protein 27, transcript variant X1
tetratricopeptide repeat protein 27 isoform X2
tetratricopeptide repeat protein 27 isoform X1
DNA helicase MCM9-like, transcript variant X1
DNA helicase MCM9-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
twisted gastrulation protein homolog 1-A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclic AMP-responsive element-binding protein 3-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
furin-like protease 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
furin-like protease 1, transcript variant X2
furin-like protease 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
furin-like protease 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
cytochrome P450 4C1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
cytochrome P450 4C1-like, transcript variant X1
cytochrome P450 4C1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myogenesis-regulating glycosidase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myogenesis-regulating glycosidase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
myogenesis-regulating glycosidase isoform X1
myogenesis-regulating glycosidase isoform X2
tubulin polyglutamylase TTLL13-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
tubulin polyglutamylase TTLL13-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tubulin polyglutamylase TTLL13-like, transcript variant X3
tubulin polyglutamylase TTLL13-like, transcript variant X1
tubulin polyglutamylase TTLL13-like isoform X2
tubulin polyglutamylase TTLL13-like, transcript variant X2
tubulin polyglutamylase TTLL13-like isoform X1
uncharacterized LOC124412921, transcript variant X2
uncharacterized LOC124412921, transcript variant X1
uncharacterized LOC124412921, transcript variant X4
uncharacterized LOC124412921, transcript variant X3
uncharacterized protein LOC124412921 isoform X1
uncharacterized protein LOC124412921 isoform X2
mitochondrial import inner membrane translocase subunit TIM50-C-like
mitochondrial mRNA pseudouridine synthase RPUSD3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
39S ribosomal protein L34, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 512B-like, transcript variant X2
zinc finger protein 512B-like isoform X2
zinc finger protein 512B-like, transcript variant X1
zinc finger protein 512B-like isoform X1
alpha-(1,6)-fucosyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
alpha-(1,6)-fucosyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
alpha-(1,6)-fucosyltransferase isoform X1
alpha-(1,6)-fucosyltransferase isoform X2
arylalkylamine N-acetyltransferase 1-like, transcript variant X2
arylalkylamine N-acetyltransferase 1-like, transcript variant X1
arylalkylamine N-acetyltransferase 1-like isoform X1
arylalkylamine N-acetyltransferase 1-like isoform X2
fasciculation and elongation protein zeta-2, transcript variant X1
fasciculation and elongation protein zeta-2, transcript variant X2
fasciculation and elongation protein zeta-2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
fasciculation and elongation protein zeta-2, transcript variant X4
fasciculation and elongation protein zeta-2 isoform X4
fasciculation and elongation protein zeta-2 isoform X1
fasciculation and elongation protein zeta-2 isoform X2
fasciculation and elongation protein zeta-2 isoform X3
M-phase inducer phosphatase-like, transcript variant X1
M-phase inducer phosphatase-like, transcript variant X2
M-phase inducer phosphatase-like, transcript variant X3
M-phase inducer phosphatase-like, transcript variant X4
M-phase inducer phosphatase-like isoform X1
M-phase inducer phosphatase-like isoform X2
phosphatidylethanolamine-binding protein homolog F40A3.3-like, transcript variant X4
phosphatidylethanolamine-binding protein homolog F40A3.3-like, transcript variant X2
phosphatidylethanolamine-binding protein homolog F40A3.3-like, transcript variant X3
phosphatidylethanolamine-binding protein homolog F40A3.3-like, transcript variant X1
phosphatidylethanolamine-binding protein homolog F40A3.3-like isoform X3
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase, transcript variant X5
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase isoform X4
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase, transcript variant X3
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase, transcript variant X1
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase, transcript variant X4
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase, transcript variant X2
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase isoform X3
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase isoform X1
alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase isoform X2
uncharacterized LOC124413036, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC124413036, transcript variant X3
uncharacterized LOC124413036, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
uncharacterized protein LOC124413036 isoform X1
uncharacterized protein LOC124413036 isoform X2
uncharacterized protein LOC124413036 isoform X3
histone RNA hairpin-binding protein, transcript variant X1
histone RNA hairpin-binding protein, transcript variant X2
uncharacterized protein LOC124413037 isoform X1
histone RNA hairpin-binding protein isoform X2
histone RNA hairpin-binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC124413037 isoform X3
ras-like protein 1, transcript variant X1
ras-like protein 1, transcript variant X2
histone-lysine N-methyltransferase ash1, transcript variant X5
histone-lysine N-methyltransferase ash1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
histone-lysine N-methyltransferase ash1, transcript variant X6
histone-lysine N-methyltransferase ash1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
histone-lysine N-methyltransferase ash1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histone-lysine N-methyltransferase ash1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
histone-lysine N-methyltransferase ash1 isoform X2
histone-lysine N-methyltransferase ash1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
uroporphyrinogen-III synthase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uroporphyrinogen-III synthase-like, transcript variant X1
SKI family transcriptional corepressor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 3-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 3-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 3-like isoform X1
ubiquitin carboxyl-terminal hydrolase 3-like isoform X2
furin-like protease 2, transcript variant X1
furin-like protease 2, transcript variant X2
protein fem-1 homolog CG6966, transcript variant X2
protein fem-1 homolog CG6966, transcript variant X1
unconventional myosin-IXAa-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
unconventional myosin-IXAa-like, transcript variant X2
unconventional myosin-IXAa-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
unconventional myosin-IXAa-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
unconventional myosin-IXAa-like, transcript variant X5
unconventional myosin-IXa-like isoform X1
unconventional myosin-IXa-like isoform X2
unconventional myosin-IXAa-like isoform X4
unconventional myosin-IXa-like isoform X3
unconventional myosin-IXAa-like isoform X5
hemicentin-2-like, transcript variant X1
hemicentin-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
integrator complex subunit 3, transcript variant X2
integrator complex subunit 3, transcript variant X3
integrator complex subunit 3, transcript variant X1
dnaJ homolog subfamily C member 3 homolog
RNA polymerase II elongation factor Ell, transcript variant X2
RNA polymerase II elongation factor Ell, transcript variant X1
uncharacterized LOC124413265, transcript variant X9
uncharacterized LOC124413265, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124413265, transcript variant X10
uncharacterized LOC124413265, transcript variant X5
uncharacterized LOC124413265, transcript variant X4
uncharacterized LOC124413265, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124413265, transcript variant X11
uncharacterized LOC124413265, transcript variant X3
uncharacterized LOC124413265, transcript variant X1
uncharacterized LOC124413265, transcript variant X7
uncharacterized LOC124413265, transcript variant X2
uncharacterized protein LOC124413265 isoform X9
uncharacterized protein LOC124413265 isoform X6
uncharacterized protein LOC124413265 isoform X10
uncharacterized protein LOC124413265 isoform X5
uncharacterized protein LOC124413265 isoform X4
uncharacterized protein LOC124413265 isoform X8
uncharacterized protein LOC124413265 isoform X11
uncharacterized protein LOC124413265 isoform X3
uncharacterized protein LOC124413265 isoform X1
uncharacterized protein LOC124413265 isoform X7
uncharacterized protein LOC124413265 isoform X2
phorbol ester/diacylglycerol-binding protein unc-13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
probable isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
phosphatidylinositol 3-kinase catalytic subunit type 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 86 samples with support for all annotated introns
uncharacterized LOC124413129, transcript variant X1
uncharacterized LOC124413129, transcript variant X2
uncharacterized protein LOC124413129 isoform X1
uncharacterized protein LOC124413129 isoform X2
uncharacterized LOC124413405, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC124413405, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC124413398, transcript variant X1
uncharacterized LOC124413398, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and death domain-containing protein 1A-like, transcript variant X3
ankyrin repeat and death domain-containing protein 1A-like, transcript variant X1
ankyrin repeat and death domain-containing protein 1A-like, transcript variant X4
ankyrin repeat and death domain-containing protein 1A-like, transcript variant X5
ankyrin repeat and death domain-containing protein 1A-like, transcript variant X2
ankyrin repeat and death domain-containing protein 1A-like isoform X1
ankyrin repeat and death domain-containing protein 1A-like isoform X2
ankyrin repeat and death domain-containing protein 1A-like isoform X3
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein 27C-like isoform X5
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X7
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein 27C-like isoform X3
heterogeneous nuclear ribonucleoprotein 27C-like isoform X7
heterogeneous nuclear ribonucleoprotein 27C-like isoform X1
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein 27C-like isoform X2
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein 27C-like isoform X4
heterogeneous nuclear ribonucleoprotein 27C-like, transcript variant X6
heterogeneous nuclear ribonucleoprotein 27C-like isoform X6
chondroitin sulfate synthase 1, transcript variant X1
chondroitin sulfate synthase 1, transcript variant X2
chondroitin sulfate synthase 1 isoform X1
chondroitin sulfate synthase 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
putative glycine-rich cell wall structural protein 1
immediate early response 3-interacting protein 1
bumetanide-sensitive sodium-(potassium)-chloride cotransporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X1
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X3
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X4
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X5
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X2
bumetanide-sensitive sodium-(potassium)-chloride cotransporter, transcript variant X6
ATP-dependent (S)-NAD(P)H-hydrate dehydratase
regulator of nonsense transcripts 1 homolog
poly(A) RNA polymerase gld-2 homolog A-like, transcript variant X3
poly(A) RNA polymerase gld-2 homolog A-like, transcript variant X1
poly(A) RNA polymerase gld-2 homolog A-like, transcript variant X2
poly(A) RNA polymerase gld-2 homolog A-like isoform X2
poly(A) RNA polymerase gld-2 homolog A-like isoform X1
poly(A) RNA polymerase gld-2 homolog A-like, transcript variant X4
poly(A) RNA polymerase gld-2 homolog B-like isoform X3
U3 small nucleolar RNA-associated protein 6 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
3-phosphoinositide-dependent protein kinase 1, transcript variant X2
3-phosphoinositide-dependent protein kinase 1, transcript variant X1
3-phosphoinositide-dependent protein kinase 1 isoform X1
3-phosphoinositide-dependent protein kinase 1 isoform X2
uncharacterized LOC124413582, transcript variant X3
uncharacterized protein LOC124413582 isoform X3
uncharacterized LOC124413582, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein LOC124413582 isoform X2
uncharacterized LOC124413582, transcript variant X1
uncharacterized protein LOC124413582 isoform X1
myocardin-related transcription factor A-like, transcript variant X1
myocardin-related transcription factor A-like, transcript variant X2
myocardin-related transcription factor A-like isoform X1
AF4/FMR2 family member lilli-like isoform X2
myocardin-related transcription factor A-like, transcript variant X3
myocardin-related transcription factor A-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
uncharacterized LOC124413252, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC124413252, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC124413252, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable 39S ribosomal protein L49, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
protein angel homolog 2, transcript variant X4
protein angel homolog 2, transcript variant X1
protein angel homolog 2, transcript variant X3
protein angel homolog 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
regulator of G-protein signaling loco, transcript variant X3
regulator of G-protein signaling loco, transcript variant X2
regulator of G-protein signaling loco, transcript variant X1
regulator of G-protein signaling loco isoform X1
regulator of G-protein signaling loco isoform X3
regulator of G-protein signaling loco isoform X2
X-ray repair cross-complementing protein 5-like
protein lin-52 homolog, transcript variant X1
protein lin-52 homolog, transcript variant X6
protein lin-52 homolog, transcript variant X4
protein lin-52 homolog, transcript variant X5
protein lin-52 homolog, transcript variant X3
protein lin-52 homolog, transcript variant X2
signal recognition particle receptor subunit alpha homolog, transcript variant X1
signal recognition particle receptor subunit alpha homolog, transcript variant X2
signal recognition particle receptor subunit alpha homolog isoform X1
signal recognition particle receptor subunit alpha homolog isoform X2
ammonium transporter Rh type A, transcript variant X3
ammonium transporter Rh type A, transcript variant X2
ammonium transporter Rh type A, transcript variant X1
ammonium transporter Rh type A isoform X2
ammonium transporter Rh type A isoform X3
ammonium transporter Rh type A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
glycogen synthase kinase-3 beta, transcript variant X5
glycogen synthase kinase-3 beta, transcript variant X3
glycogen synthase kinase-3 beta isoform X5
glycogen synthase kinase-3 beta isoform X3
glycogen synthase kinase-3 beta, transcript variant X2
glycogen synthase kinase-3 beta, transcript variant X4
glycogen synthase kinase-3 beta, transcript variant X1
glycogen synthase kinase-3 beta isoform X2
glycogen synthase kinase-3 beta isoform X1
glycogen synthase kinase-3 beta isoform X4
leucine-rich repeat-containing protein 58, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
leucine-rich repeat-containing protein 58, transcript variant X2
leucine-rich repeat-containing protein 58, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
leucine-rich repeat-containing protein 58
mitochondrial ribonuclease P catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
general odorant-binding protein 72-like, transcript variant X6
general odorant-binding protein 72-like, transcript variant X1
general odorant-binding protein 72-like, transcript variant X5
general odorant-binding protein 72-like, transcript variant X2
general odorant-binding protein 72-like, transcript variant X3
general odorant-binding protein 72-like, transcript variant X4
general odorant-binding protein 72-like, transcript variant X7
general odorant-binding protein 72-like isoform X1
general odorant-binding protein 72-like isoform X2
eukaryotic translation initiation factor 2-alpha kinase 3-like
39S ribosomal protein L43, mitochondrial, transcript variant X2
39S ribosomal protein L43, mitochondrial, transcript variant X1
39S ribosomal protein L43, mitochondrial
aldo-keto reductase family 1 member B1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
aldo-keto reductase family 1 member B1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
aldo-keto reductase family 1 member B1-like isoform X1
aldo-keto reductase family 1 member B1-like isoform X2
aldo-keto reductase family 1 member B1-like
glucosamine-6-phosphate isomerase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
E3 ubiquitin-protein ligase RMND5A, transcript variant X1
E3 ubiquitin-protein ligase RMND5A, transcript variant X2
E3 ubiquitin-protein ligase RMND5A isoform X1
E3 ubiquitin-protein ligase RMND5A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59% coverage of the annotated genomic feature by RNAseq alignments
synaptic vesicular amine transporter, transcript variant X2
synaptic vesicular amine transporter, transcript variant X3
synaptic vesicular amine transporter, transcript variant X1
synaptic vesicular amine transporter isoform X1
synaptic vesicular amine transporter isoform X2
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
odorant receptor 49b-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
odorant receptor 49b-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
dynein regulatory complex subunit 5-like, transcript variant X1
dynein regulatory complex subunit 5-like, transcript variant X2
dynein regulatory complex subunit 5-like isoform X1
dynein regulatory complex subunit 5-like isoform X2
translation initiation factor eIF-2B subunit beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 79 samples with support for all annotated introns
uncharacterized LOC124413276, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC124413276, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC124413276 isoform X2
uncharacterized protein LOC124413276 isoform X1
uncharacterized LOC124413276, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein LOC124413276 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
protein neuralized, transcript variant X3
protein neuralized, transcript variant X1
protein neuralized, transcript variant X2
protein neuralized, transcript variant X4
protein unc-13 homolog 4B, transcript variant X3
protein unc-13 homolog 4B, transcript variant X1
protein unc-13 homolog 4B, transcript variant X2
protein unc-13 homolog 4B, transcript variant X4
protein unc-13 homolog 4B, transcript variant X5
protein unc-13 homolog 4B, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
protein abrupt-like, transcript variant X2
protein abrupt-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
protein abrupt-like, transcript variant X3
protein abrupt-like, transcript variant X5
protein abrupt-like, transcript variant X4
actin-interacting protein 1, transcript variant X1
actin-interacting protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
cilia- and flagella-associated protein 161-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 16% coverage of the annotated genomic feature by RNAseq alignments
glyoxylate reductase/hydroxypyruvate reductase
adipokinetic hormone/corazonin-related peptide-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
exocyst complex component 4, transcript variant X2
exocyst complex component 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 460 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein ZK1073.1, transcript variant X3
uncharacterized protein ZK1073.1, transcript variant X1
uncharacterized protein ZK1073.1, transcript variant X2
uncharacterized protein ZK1073.1, transcript variant X4
uncharacterized protein ZK1073.1 isoform X2
uncharacterized protein ZK1073.1 isoform X1
uncharacterized protein ZK1073.1 isoform X3
golgin subfamily A member 6-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
hematopoietically-expressed homeobox protein hhex
protein couch potato, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein couch potato, transcript variant X2
protein couch potato, transcript variant X3
protein couch potato, transcript variant X4
U1 small nuclear ribonucleoprotein A isoform X2
U1 small nuclear ribonucleoprotein A isoform X1
KAT8 regulatory NSL complex subunit 1, transcript variant X3
KAT8 regulatory NSL complex subunit 1, transcript variant X1
KAT8 regulatory NSL complex subunit 1, transcript variant X2
KAT8 regulatory NSL complex subunit 1 isoform X2
KAT8 regulatory NSL complex subunit 1 isoform X1
KAT8 regulatory NSL complex subunit 1 isoform X3
small G protein signaling modulator 3 homolog
succinate dehydrogenase assembly factor 4, mitochondrial-like, transcript variant X1
succinate dehydrogenase assembly factor 4, mitochondrial-like, transcript variant X2
succinate dehydrogenase assembly factor 4, mitochondrial-like isoform X1
succinate dehydrogenase assembly factor 4, mitochondrial-like isoform X2
protein polybromo-1, transcript variant X2
protein polybromo-1, transcript variant X8
protein polybromo-1, transcript variant X7
protein polybromo-1, transcript variant X5
protein polybromo-1, transcript variant X4
protein polybromo-1, transcript variant X6
protein polybromo-1, transcript variant X1
protein polybromo-1, transcript variant X3
uncharacterized LOC124413539, transcript variant X5
uncharacterized LOC124413539, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC124413539, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC124413539, transcript variant X2
uncharacterized LOC124413539, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
proline-rich nuclear receptor coactivator 2-like
E3 ubiquitin-protein ligase RNF38-like, transcript variant X1
E3 ubiquitin-protein ligase RNF38-like, transcript variant X3
E3 ubiquitin-protein ligase RNF38-like, transcript variant X2
E3 ubiquitin-protein ligase RNF38-like isoform X2
E3 ubiquitin-protein ligase RNF38-like isoform X1
coiled-coil domain-containing protein 186, transcript variant X2
coiled-coil domain-containing protein 186, transcript variant X1
coiled-coil domain-containing protein 186 isoform X2
coiled-coil domain-containing protein 186 isoform X1
coiled-coil domain-containing protein 186, transcript variant X3
coiled-coil domain-containing protein 186 isoform X3
arrestin domain-containing protein 17, transcript variant X2
arrestin domain-containing protein 17, transcript variant X1
arrestin domain-containing protein 17 isoform X2
arrestin domain-containing protein 17 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
eukaryotic peptide chain release factor subunit 1, transcript variant X3
eukaryotic peptide chain release factor subunit 1, transcript variant X2
eukaryotic peptide chain release factor subunit 1, transcript variant X1
eukaryotic peptide chain release factor subunit 1 isoform X1
eukaryotic peptide chain release factor subunit 1 isoform X2
actin-related protein 2/3 complex subunit 1A-B, transcript variant X1
actin-related protein 2/3 complex subunit 1A-B, transcript variant X2
actin-related protein 2/3 complex subunit 1A-B isoform X1
actin-related protein 2/3 complex subunit 1A-B isoform X2
death-associated protein kinase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
death-associated protein kinase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
death-associated protein kinase 1-like isoform X1
death-associated protein kinase 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
B-cell lymphoma/leukemia 11A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
B-cell lymphoma/leukemia 11A, transcript variant X3
B-cell lymphoma/leukemia 11A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
B-cell lymphoma/leukemia 11A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC124413530, transcript variant X4
uncharacterized LOC124413530, transcript variant X2
uncharacterized LOC124413530, transcript variant X3
uncharacterized LOC124413530, transcript variant X1
uncharacterized protein LOC124413530 isoform X1
uncharacterized protein LOC124413530 isoform X2
muscle M-line assembly protein unc-89, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
muscle M-line assembly protein unc-89, transcript variant X1
muscle M-line assembly protein unc-89 isoform X1
muscle M-line assembly protein unc-89, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
muscle M-line assembly protein unc-89, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
muscle M-line assembly protein unc-89, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
muscle M-line assembly protein unc-89 isoform X2
muscle M-line assembly protein unc-89 isoform X3
tubulin-specific chaperone cofactor E-like protein, transcript variant X2
tubulin-specific chaperone cofactor E-like protein, transcript variant X4
tubulin-specific chaperone cofactor E-like protein, transcript variant X3
tubulin-specific chaperone cofactor E-like protein, transcript variant X5
tubulin-specific chaperone cofactor E-like protein, transcript variant X1
tubulin-specific chaperone cofactor E-like protein isoform X1
tubulin-specific chaperone cofactor E-like protein isoform X2
zinc finger matrin-type protein CG9776-like, transcript variant X1
zinc finger matrin-type protein CG9776-like, transcript variant X3
zinc finger matrin-type protein CG9776-like, transcript variant X2
zinc finger matrin-type protein CG9776-like isoform X1
zinc finger matrin-type protein CG9776-like isoform X2
ADP-dependent glucokinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
ADP-dependent glucokinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
cyclin-dependent kinase 2-interacting protein
uncharacterized LOC124412891, transcript variant X3
uncharacterized protein LOC124412891 isoform X3
uncharacterized LOC124412891, transcript variant X1
uncharacterized protein LOC124412891 isoform X1
uncharacterized LOC124412891, transcript variant X2
uncharacterized protein LOC124412891 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 81 samples with support for all annotated introns
ejaculatory bulb-specific protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
ejaculatory bulb-specific protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 79 samples with support for all annotated introns
ejaculatory bulb-specific protein 3-like
DENN domain-containing protein Crag, transcript variant X1
DENN domain-containing protein Crag, transcript variant X2
DENN domain-containing protein Crag, transcript variant X7
DENN domain-containing protein Crag, transcript variant X5
DENN domain-containing protein Crag, transcript variant X4
DENN domain-containing protein Crag, transcript variant X3
DENN domain-containing protein 4C isoform X1
DENN domain-containing protein Crag isoform X4
DENN domain-containing protein 4C isoform X3
DENN domain-containing protein 4C isoform X2
DENN domain-containing protein Crag isoform X6
DENN domain-containing protein Crag, transcript variant X6
DENN domain-containing protein 4C isoform X5
dynein regulatory complex protein 10-like, transcript variant X2
dynein regulatory complex protein 10-like, transcript variant X1
dynein regulatory complex protein 10-like isoform X2
dynein regulatory complex protein 10-like isoform X1
arrestin domain-containing protein 17-like, transcript variant X2
arrestin domain-containing protein 17-like, transcript variant X1
arrestin domain-containing protein 17-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 29% coverage of the annotated genomic feature by RNAseq alignments
LHFPL tetraspan subfamily member 6 protein-like
band 7 protein AGAP004871-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
band 7 protein AGAP004871-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
band 7 protein AGAP004871-like isoform X1
band 7 protein AGAP004871-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
leucine-rich repeat transmembrane neuronal protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
cytosol aminopeptidase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 53 samples with support for all annotated introns
cytosol aminopeptidase-like, transcript variant X4
cytosol aminopeptidase-like, transcript variant X2
cytosol aminopeptidase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
cytosol aminopeptidase-like, transcript variant X5
E3 ubiquitin-protein ligase COP1-like isoform X1
mediator of RNA polymerase II transcription subunit 28
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
sodium channel protein para, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium channel protein para, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein para, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium channel protein para, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium channel protein para, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein para, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein para, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium channel protein para, transcript variant X4
sodium channel protein para, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein para, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium channel protein para, transcript variant X12
sodium channel protein para, transcript variant X11
sodium channel protein para, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium channel protein para, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium channel protein para, transcript variant X16
sodium channel protein para, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel protein para, transcript variant X1
sodium channel protein para, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
small conductance calcium-activated potassium channel protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
small conductance calcium-activated potassium channel protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
small conductance calcium-activated potassium channel protein isoform X1
small conductance calcium-activated potassium channel protein isoform X2
small conductance calcium-activated potassium channel protein, transcript variant X3
small conductance calcium-activated potassium channel protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
glycosylated lysosomal membrane protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124413377, transcript variant X2
uncharacterized LOC124413377, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 259 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: acetylcholine receptor subunit alpha-like 1
acetylcholine receptor subunit alpha-L1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 269 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
acetylcholine receptor subunit alpha-L1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 269 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acetylcholine receptor subunit beta-like 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 279 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
acetylcholine receptor subunit beta-like 2
acetylcholine receptor subunit beta-like 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 262 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 1 isoform X1
conserved oligomeric Golgi complex subunit 1 isoform X2
tyrosine-protein phosphatase non-receptor type 9, transcript variant X2
tyrosine-protein phosphatase non-receptor type 9 isoform X2
tyrosine-protein phosphatase non-receptor type 9, transcript variant X1
tyrosine-protein phosphatase non-receptor type 9 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 2-alpha kinase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uncharacterized LOC124413164, transcript variant X1
uncharacterized LOC124413164, transcript variant X2
uncharacterized protein LOC124413164 isoform X1
uncharacterized protein LOC124413164 isoform X2
uncharacterized LOC124412874, transcript variant X3
uncharacterized LOC124412874, transcript variant X4
uncharacterized LOC124412874, transcript variant X5
uncharacterized LOC124412874, transcript variant X6
uncharacterized LOC124412874, transcript variant X2
uncharacterized LOC124412874, transcript variant X1
uncharacterized protein LOC124412874 isoform X3
uncharacterized protein LOC124412874 isoform X4
uncharacterized protein LOC124412874 isoform X5
uncharacterized protein LOC124412874 isoform X6
uncharacterized protein LOC124412874 isoform X2
uncharacterized protein LOC124412874 isoform X1
uncharacterized LOC124413249, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
uncharacterized LOC124413249, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
uncharacterized protein LOC124413249 isoform X1
uncharacterized protein LOC124413249 isoform X2
hypoxia up-regulated protein 1, transcript variant X2
hypoxia up-regulated protein 1, transcript variant X1
hypoxia up-regulated protein 1 isoform X2
hypoxia up-regulated protein 1 isoform X1
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
probable E3 ubiquitin-protein ligase IRF2BPL, transcript variant X1
probable E3 ubiquitin-protein ligase IRF2BPL, transcript variant X2
interferon regulatory factor 2-binding protein 1 isoform X1
probable E3 ubiquitin-protein ligase IRF2BPL isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61% coverage of the annotated genomic feature by RNAseq alignments
inositol-tetrakisphosphate 1-kinase-like
39S ribosomal protein L33, mitochondrial
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
HMG box transcription factor BBX, transcript variant X1
HMG box transcription factor BBX, transcript variant X2
HMG box transcription factor BBX, transcript variant X4
HMG box transcription factor BBX, transcript variant X3
uncharacterized protein LOC124413105 isoform X1
uncharacterized protein LOC124413105 isoform X2
HMG box transcription factor BBX isoform X4
uncharacterized protein LOC124413105 isoform X3
uncharacterized LOC124413223, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC124413223, transcript variant X3
uncharacterized LOC124413223, transcript variant X2
uncharacterized protein LOC124413223 isoform X3
uncharacterized protein LOC124413223 isoform X2
uncharacterized protein LOC124413223 isoform X1
protein Smaug homolog 1, transcript variant X3
protein Smaug homolog 1, transcript variant X4
protein Smaug homolog 1, transcript variant X1
protein Smaug homolog 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124413221, transcript variant X1
uncharacterized protein LOC124413221 isoform X1
uncharacterized LOC124413221, transcript variant X2
uncharacterized protein LOC124413221 isoform X2
uncharacterized LOC124413222, transcript variant X1
uncharacterized LOC124413222, transcript variant X2
uncharacterized protein LOC124413222 isoform X2
uncharacterized protein LOC124413222 isoform X1
uncharacterized protein DDB_G0271670-like, transcript variant X7
uncharacterized protein DDB_G0271670-like, transcript variant X5
uncharacterized protein DDB_G0271670-like, transcript variant X6
uncharacterized protein DDB_G0271670-like, transcript variant X4
uncharacterized protein DDB_G0271670-like, transcript variant X3
uncharacterized protein DDB_G0271670-like, transcript variant X1
uncharacterized protein DDB_G0271670-like, transcript variant X2
uncharacterized protein DDB_G0271670-like isoform X3
uncharacterized protein DDB_G0271670-like isoform X1
uncharacterized protein DDB_G0271670-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
small nucleolar RNA snR60/Z15/Z230/Z193/J17
COORDINATES: nucleotide motif:Rfam:12.0:RF00309
D-beta-hydroxybutyrate dehydrogenase, mitochondrial
adult-specific cuticular protein ACP-22-like
kin of IRRE-like protein 1, transcript variant X1
kin of IRRE-like protein 1, transcript variant X3
kin of IRRE-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 79 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
V-type proton ATPase catalytic subunit A
probable 39S ribosomal protein L45, mitochondrial
oxysterol-binding protein-related protein 11, transcript variant X1
oxysterol-binding protein-related protein 11, transcript variant X2
oxysterol-binding protein-related protein 11 isoform X2
oxysterol-binding protein-related protein 11 isoform X1
uncharacterized LOC124413211, transcript variant X2
uncharacterized LOC124413211, transcript variant X1
uncharacterized protein LOC124413211 isoform X2
uncharacterized protein LOC124413211 isoform X1
putative U5 small nuclear ribonucleoprotein 200 kDa helicase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
janus kinase and microtubule-interacting protein 3-like, transcript variant X1
janus kinase and microtubule-interacting protein 3-like, transcript variant X3
janus kinase and microtubule-interacting protein 3-like, transcript variant X2
janus kinase and microtubule-interacting protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
U6 snRNA-associated Sm-like protein LSm1
uncharacterized LOC124413524, transcript variant X2
uncharacterized LOC124413524, transcript variant X1
uncharacterized protein LOC124413524 isoform X2
uncharacterized protein LOC124413524 isoform X1
uncharacterized LOC124413523, transcript variant X3
uncharacterized LOC124413523, transcript variant X1
uncharacterized LOC124413523, transcript variant X2
uncharacterized protein LOC124413523 isoform X1
uncharacterized protein LOC124413523 isoform X2
uncharacterized protein LOC124413523 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor receptor homolog 1-like, transcript variant X1
fibroblast growth factor receptor homolog 1-like, transcript variant X3
fibroblast growth factor receptor homolog 1-like, transcript variant X2
fibroblast growth factor receptor homolog 1-like isoform X1
fibroblast growth factor receptor homolog 1-like isoform X2
polycomb group RING finger protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
polycomb group RING finger protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
polycomb group RING finger protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124413319, transcript variant X2
uncharacterized LOC124413319, transcript variant X1
uncharacterized protein LOC124413319 isoform X1
uncharacterized protein LOC124413319 isoform X2
signal recognition particle subunit SRP72
general odorant-binding protein 83a-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC124413322
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 55% coverage of the annotated genomic feature by RNAseq alignments
general odorant-binding protein 69a-like, transcript variant X1
general odorant-binding protein 69a-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
general odorant-binding protein 69a-like isoform X2
general odorant-binding protein 56d-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
dipeptidyl peptidase 9, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
39S ribosomal protein L51, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
dipeptidyl peptidase 9, transcript variant X4
dipeptidyl peptidase 9, transcript variant X1
dipeptidyl peptidase 9, transcript variant X5
dipeptidyl peptidase 9, transcript variant X3
dipeptidyl peptidase 9, transcript variant X2
dipeptidyl peptidase 9, transcript variant X7
RNA-binding protein Musashi homolog 2-like, transcript variant X1
RNA-binding protein Musashi homolog 2-like, transcript variant X4
RNA-binding protein Musashi homolog 2-like, transcript variant X3
RNA-binding protein Musashi homolog 2-like, transcript variant X2
RNA-binding protein Musashi homolog 2-like, transcript variant X7
RNA-binding protein Musashi homolog 2-like, transcript variant X5
RNA-binding protein Musashi homolog 2-like, transcript variant X6
RNA-binding protein Musashi homolog 2-like isoform X1
RNA-binding protein Musashi homolog 2-like isoform X3
RNA-binding protein Musashi homolog 2-like isoform X2
RNA-binding protein Musashi homolog 2-like isoform X4
RNA-binding protein Musashi homolog 2-like isoform X5
RNA-binding protein Musashi homolog 2-like isoform X6
proteasome subunit alpha type-2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
proteasome subunit alpha type-2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
proteasome subunit alpha type-2, transcript variant X1
interleukin enhancer-binding factor 2, transcript variant X2
interleukin enhancer-binding factor 2, transcript variant X1
interleukin enhancer-binding factor 2 isoform X1
interleukin enhancer-binding factor 2 isoform X2
uncharacterized LOC124413494, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC124413494 isoform X1
uncharacterized LOC124413494, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC124413494 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 3C, transcript variant X2
protein phosphatase 1 regulatory subunit 3C, transcript variant X3
protein phosphatase 1 regulatory subunit 3C, transcript variant X1
protein phosphatase 1 regulatory subunit 3C isoform X2
protein phosphatase 1 regulatory subunit 3C isoform X1
poly [ADP-ribose] polymerase tankyrase, transcript variant X2
poly [ADP-ribose] polymerase tankyrase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
poly [ADP-ribose] polymerase tankyrase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
poly [ADP-ribose] polymerase tankyrase isoform X3
poly [ADP-ribose] polymerase tankyrase isoform X2
poly [ADP-ribose] polymerase tankyrase isoform X1
cytoplasmic aconitate hydratase-like, transcript variant X3
cytoplasmic aconitate hydratase-like isoform X3
cytoplasmic aconitate hydratase-like, transcript variant X1
cytoplasmic aconitate hydratase-like isoform X1
cytoplasmic aconitate hydratase-like, transcript variant X2
cytoplasmic aconitate hydratase-like isoform X2
tight junction protein ZO-1, transcript variant X1
tight junction protein ZO-1, transcript variant X2
tight junction protein ZO-1, transcript variant X6
tight junction protein ZO-1, transcript variant X7
tight junction protein ZO-1, transcript variant X8
tight junction protein ZO-1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
tight junction protein ZO-1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
tight junction protein ZO-1, transcript variant X5
tight junction protein ZO-1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
another transcription unit protein, transcript variant X1
another transcription unit protein, transcript variant X2
another transcription unit protein, transcript variant X3
another transcription unit protein, transcript variant X4
another transcription unit protein isoform X1
another transcription unit protein isoform X2
another transcription unit protein isoform X3
another transcription unit protein isoform X4
sterol carrier protein 2-like, transcript variant X1
sterol carrier protein 2-like, transcript variant X3
sterol carrier protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
sortilin-related receptor-like, transcript variant X2
sortilin-related receptor-like, transcript variant X1
sortilin-related receptor-like, transcript variant X4
sortilin-related receptor-like isoform X2
sortilin-related receptor-like isoform X1
sortilin-related receptor-like isoform X4
sortilin-related receptor-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sortilin-related receptor-like isoform X3
spectrin beta chain, transcript variant X6
spectrin beta chain, transcript variant X7
spectrin beta chain, transcript variant X4
spectrin beta chain, transcript variant X5
spectrin beta chain, transcript variant X3
spectrin beta chain, transcript variant X2
spectrin beta chain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
vam6/Vps39-like protein, transcript variant X2
vam6/Vps39-like protein, transcript variant X1
N-alpha-acetyltransferase 38, NatC auxiliary subunit
H/ACA ribonucleoprotein complex non-core subunit NAF1
putative ATP-dependent RNA helicase DHX57, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
putative ATP-dependent RNA helicase DHX57, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
putative ATP-dependent RNA helicase DHX57, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
putative ATP-dependent RNA helicase DHX57 isoform X1
putative ATP-dependent RNA helicase DHX57 isoform X2
putative ATP-dependent RNA helicase DHX57, transcript variant X4
putative ATP-dependent RNA helicase DHX57 isoform X3
amyloid-beta-like protein, transcript variant X2
amyloid-beta-like protein, transcript variant X3
amyloid-beta-like protein, transcript variant X1
persulfide dioxygenase ETHE1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
serine/threonine-protein kinase SIK2-like
39S ribosomal protein L41, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
tRNA pseudouridine synthase A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
tRNA pseudouridine synthase A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
tRNA pseudouridine synthase A isoform X1
tRNA pseudouridine synthase A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124413710, transcript variant X1
uncharacterized protein LOC124413710 isoform X1
uncharacterized LOC124413710, transcript variant X2
uncharacterized protein LOC124413710 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: modular serine protease-like
mannan-binding lectin serine protease 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
charged multivesicular body protein 7, transcript variant X3
charged multivesicular body protein 7, transcript variant X1
charged multivesicular body protein 7, transcript variant X2
charged multivesicular body protein 7 isoform X1
charged multivesicular body protein 7 isoform X2
erythroid differentiation-related factor 1, transcript variant X2
erythroid differentiation-related factor 1, transcript variant X1
erythroid differentiation-related factor 1 isoform X1
erythroid differentiation-related factor 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
galactoside 2-alpha-L-fucosyltransferase Sec1-like, transcript variant X1
galactoside 2-alpha-L-fucosyltransferase Sec1-like, transcript variant X2
galactoside 2-alpha-L-fucosyltransferase Sec1-like
pantothenate kinase 3, transcript variant X4
pantothenate kinase 3, transcript variant X1
pantothenate kinase 3, transcript variant X5
pantothenate kinase 3, transcript variant X3
pantothenate kinase 3, transcript variant X2
pantothenate kinase 3, transcript variant X6
pantothenate kinase 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
MORN repeat-containing protein 4 homolog, transcript variant X1
MORN repeat-containing protein 4 homolog, transcript variant X2
MORN repeat-containing protein 4 homolog isoform X2
MORN repeat-containing protein 4 homolog isoform X1
MMS19 nucleotide excision repair protein
ubiquitin domain-containing protein 1, transcript variant X1
ubiquitin domain-containing protein 1, transcript variant X2
cytochrome c oxidase assembly protein COX15 homolog, transcript variant X2
cytochrome c oxidase assembly protein COX15 homolog, transcript variant X1
cytochrome c oxidase assembly protein COX15 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 416 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
double-stranded RNA-specific editase Adar, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
double-stranded RNA-specific editase Adar isoform X2
major facilitator superfamily domain-containing protein 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized protein LOC124412845 isoform X1
major facilitator superfamily domain-containing protein 6 isoform X2
double-stranded RNA-specific editase Adar, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
double-stranded RNA-specific editase Adar isoform X5
double-stranded RNA-specific editase Adar, transcript variant X4
double-stranded RNA-specific editase Adar isoform X4
double-stranded RNA-specific editase Adar, transcript variant X3
double-stranded RNA-specific editase Adar isoform X3
double-stranded RNA-specific editase Adar, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
double-stranded RNA-specific editase Adar isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase ATL44
glucose dehydrogenase [FAD, quinone]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
prion-like-(Q/N-rich) domain-bearing protein 25, transcript variant X2
prion-like-(Q/N-rich) domain-bearing protein 25, transcript variant X4
prion-like-(Q/N-rich) domain-bearing protein 25, transcript variant X1
prion-like-(Q/N-rich) domain-bearing protein 25 isoform X2
prion-like-(Q/N-rich) domain-bearing protein 25 isoform X4
prion-like-(Q/N-rich) domain-bearing protein 25 isoform X1
prion-like-(Q/N-rich) domain-bearing protein 25, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
prion-like-(Q/N-rich) domain-bearing protein 25 isoform X3
multiple epidermal growth factor-like domains protein 6
prion-like-(Q/N-rich) domain-bearing protein 25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00093
uncharacterized LOC124412981, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC124412981, transcript variant X1
uncharacterized LOC124412981, transcript variant X3
neuronal acetylcholine receptor subunit alpha-7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-7-like, transcript variant X2
neuronal acetylcholine receptor subunit alpha-7-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-10-like isoform X1
neuronal acetylcholine receptor subunit alpha-10-like isoform X2
neuronal acetylcholine receptor subunit alpha-7-like isoform X3
mitochondrial coenzyme A transporter SLC25A42, transcript variant X1
mitochondrial coenzyme A transporter SLC25A42, transcript variant X2
mitochondrial coenzyme A transporter SLC25A42
crossover junction endonuclease EME1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
crossover junction endonuclease EME1, transcript variant X2
crossover junction endonuclease EME1 isoform X1
crossover junction endonuclease EME1 isoform X2
KAT8 regulatory NSL complex subunit 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
KAT8 regulatory NSL complex subunit 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
KAT8 regulatory NSL complex subunit 3 isoform X1
KAT8 regulatory NSL complex subunit 3 isoform X2
transcription elongation regulator 1, transcript variant X1
transcription elongation regulator 1, transcript variant X2
transcription elongation regulator 1 isoform X1
transcription elongation regulator 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
cilia- and flagella-associated protein 43-like, transcript variant X2
cilia- and flagella-associated protein 43-like, transcript variant X1
cilia- and flagella-associated protein 43-like isoform X2
cilia- and flagella-associated protein 43-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: F-box only protein 39-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 67 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
atrial natriuretic peptide receptor 1, transcript variant X4
atrial natriuretic peptide receptor 1, transcript variant X1
atrial natriuretic peptide receptor 1, transcript variant X3
atrial natriuretic peptide receptor 1, transcript variant X2
atrial natriuretic peptide receptor 1 isoform X1
atrial natriuretic peptide receptor 1 isoform X4
atrial natriuretic peptide receptor 1 isoform X3
atrial natriuretic peptide receptor 1 isoform X2
DNA-directed primase/polymerase protein-like
stAR-related lipid transfer protein 7, mitochondrial, transcript variant X2
stAR-related lipid transfer protein 7, mitochondrial, transcript variant X3
stAR-related lipid transfer protein 7, mitochondrial, transcript variant X1
stAR-related lipid transfer protein 7, mitochondrial isoform X2
stAR-related lipid transfer protein 7, mitochondrial isoform X3
stAR-related lipid transfer protein 7, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
ornithine aminotransferase, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ornithine aminotransferase, mitochondrial-like, transcript variant X2
ornithine aminotransferase, mitochondrial-like, transcript variant X1
ornithine aminotransferase, mitochondrial-like
ornithine aminotransferase, mitochondrial
cell division cycle-associated protein 7-like
probable methyltransferase-like protein 25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
SWI/SNF complex subunit SMARCC2, transcript variant X1
SWI/SNF complex subunit SMARCC2, transcript variant X2
SWI/SNF complex subunit SMARCC2 isoform X1
SWI/SNF complex subunit SMARCC2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
signal transducer and activator of transcription 5B, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
signal transducer and activator of transcription 5B, transcript variant X4
signal transducer and activator of transcription 5B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
signal transducer and activator of transcription 5B, transcript variant X1
signal transducer and activator of transcription 5B, transcript variant X5
signal transducer and activator of transcription 5B, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
signal transducer and activator of transcription 5B, transcript variant X2
signal transducer and activator of transcription 5B isoform X1
signal transducer and activator of transcription 5B isoform X2
signal transducer and activator of transcription 5B isoform X3
signal transducer and activator of transcription 5B isoform X4
stabilizer of axonemal microtubules 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 4-kinase type 2-alpha, transcript variant X2
phosphatidylinositol 4-kinase type 2-alpha, transcript variant X1
phosphatidylinositol 4-kinase type 2-alpha isoform X2
phosphatidylinositol 4-kinase type 2-alpha isoform X1
exonuclease 3'-5' domain-containing protein 2
mitochondrial import inner membrane translocase subunit Tim16, transcript variant X2
mitochondrial import inner membrane translocase subunit Tim16, transcript variant X3
mitochondrial import inner membrane translocase subunit Tim16, transcript variant X1
mitochondrial import inner membrane translocase subunit Tim16 isoform X1
mitochondrial import inner membrane translocase subunit Tim16 isoform X2
potassium voltage-gated channel protein eag, transcript variant X1
potassium voltage-gated channel protein eag, transcript variant X8
potassium voltage-gated channel protein eag, transcript variant X6
potassium voltage-gated channel protein eag, transcript variant X9
potassium voltage-gated channel protein eag, transcript variant X5
potassium voltage-gated channel protein eag, transcript variant X7
potassium voltage-gated channel protein eag, transcript variant X10
potassium voltage-gated channel protein eag, transcript variant X4
potassium voltage-gated channel protein eag, transcript variant X2
potassium voltage-gated channel protein eag, transcript variant X3
potassium voltage-gated channel protein eag isoform X1
potassium voltage-gated channel protein eag isoform X5
potassium voltage-gated channel protein eag isoform X3
potassium voltage-gated channel protein eag isoform X6
potassium voltage-gated channel protein eag isoform X2
potassium voltage-gated channel protein eag isoform X4
potassium voltage-gated channel protein eag isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
glycine N-methyltransferase, transcript variant X1
glycine N-methyltransferase, transcript variant X3
glycine N-methyltransferase, transcript variant X4
glycine N-methyltransferase, transcript variant X2
serine/threonine-protein kinase PAK mbt, transcript variant X2
serine/threonine-protein kinase PAK mbt, transcript variant X1
ectonucleoside triphosphate diphosphohydrolase 5, transcript variant X2
ectonucleoside triphosphate diphosphohydrolase 5, transcript variant X3
ectonucleoside triphosphate diphosphohydrolase 5, transcript variant X4
ectonucleoside triphosphate diphosphohydrolase 5, transcript variant X1
ectonucleoside triphosphate diphosphohydrolase 5 isoform X2
ectonucleoside triphosphate diphosphohydrolase 5 isoform X3
ectonucleoside triphosphate diphosphohydrolase 5 isoform X1
ectonucleoside triphosphate diphosphohydrolase 5 isoform X4
mitochondrial 2-oxodicarboxylate carrier
uncharacterized LOC124413274, transcript variant X2
uncharacterized LOC124413274, transcript variant X1
uncharacterized protein LOC124413274 isoform X2
uncharacterized protein LOC124413274 isoform X1
uncharacterized protein C19orf47 homolog, transcript variant X1
uncharacterized protein C19orf47 homolog, transcript variant X2
uncharacterized protein C19orf47 homolog isoform X1
uncharacterized protein C19orf47 homolog isoform X2
alpha-actinin, sarcomeric, transcript variant X4
alpha-actinin, sarcomeric, transcript variant X2
alpha-actinin, sarcomeric, transcript variant X3
alpha-actinin, sarcomeric, transcript variant X1
mothers against decapentaplegic homolog 4, transcript variant X1
mothers against decapentaplegic homolog 4, transcript variant X4
mothers against decapentaplegic homolog 4, transcript variant X3
mothers against decapentaplegic homolog 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
mothers against decapentaplegic homolog 4 isoform X1
mothers against decapentaplegic homolog 4 isoform X4
mothers against decapentaplegic homolog 4 isoform X3
mothers against decapentaplegic homolog 4 isoform X2
probable 28S ribosomal protein S26, mitochondrial
cytoplasmic polyadenylation element-binding protein 2-like, transcript variant X2
cytoplasmic polyadenylation element-binding protein 2-like isoform X2
cytoplasmic polyadenylation element-binding protein 2-like, transcript variant X3
cytoplasmic polyadenylation element-binding protein 2-like, transcript variant X1
cytoplasmic polyadenylation element-binding protein 2-like isoform X1
cytoplasmic polyadenylation element-binding protein 2-like isoform X3
DDRGK domain-containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
DDRGK domain-containing protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
DDRGK domain-containing protein 1 isoform X1
DDRGK domain-containing protein 1 isoform X2
transmembrane emp24 domain-containing protein eca
nucleoside diphosphate kinase homolog 5-like
myogenesis-regulating glycosidase, transcript variant X3
myogenesis-regulating glycosidase isoform X3
microtubule-associated protein futsch-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
homeobox protein Nkx-2.2a-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
homeobox protein Nkx-2.2a-like isoform X2
homeobox protein Nkx-2.2a-like, transcript variant X1
homeobox protein Nkx-2.2a-like isoform X1
uncharacterized LOC124413368, transcript variant X1
uncharacterized LOC124413368, transcript variant X3
uncharacterized LOC124413368, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
uncharacterized protein LOC124413368 isoform X3
uncharacterized protein LOC124413368 isoform X1
uncharacterized protein LOC124413368 isoform X2
serine/threonine-protein phosphatase PP1-beta catalytic subunit, transcript variant X4
serine/threonine-protein phosphatase PP1-beta catalytic subunit, transcript variant X3
serine/threonine-protein phosphatase PP1-beta catalytic subunit, transcript variant X2
serine/threonine-protein phosphatase PP1-beta catalytic subunit, transcript variant X1
serine/threonine-protein phosphatase PP1-beta catalytic subunit isoform X2
serine/threonine-protein phosphatase PP1-beta catalytic subunit isoform X1
protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC124413333, transcript variant X4
uncharacterized LOC124413333, transcript variant X1
uncharacterized protein LOC124413333 isoform X1
uncharacterized LOC124413333, transcript variant X3
uncharacterized protein LOC124413333 isoform X3
uncharacterized LOC124413333, transcript variant X2
uncharacterized protein LOC124413333 isoform X2
uncharacterized protein LOC124413333 isoform X4
glutamine amidotransferase-like class 1 domain-containing protein 3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
transcription factor collier-like, transcript variant X1
transcription factor collier-like, transcript variant X2
transcription factor collier-like isoform X1
transcription factor collier-like isoform X2
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fibroblast growth factor 17, transcript variant X3
fibroblast growth factor 17, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
fibroblast growth factor 17, transcript variant X2
uncharacterized protein LOC124413331 isoform X1
uncharacterized protein LOC124413331 isoform X2
probable tyrosine-protein phosphatase F54C8.4
uncharacterized LOC124413112, transcript variant X1
uncharacterized LOC124413112, transcript variant X4
uncharacterized LOC124413112, transcript variant X3
uncharacterized LOC124413112, transcript variant X2
uncharacterized protein LOC124413112 isoform X3
uncharacterized protein LOC124413112 isoform X2
uncharacterized protein LOC124413112 isoform X1
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X2
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X4
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X3
probable JmjC domain-containing histone demethylation protein 2C isoform X2
probable JmjC domain-containing histone demethylation protein 2C isoform X4
probable JmjC domain-containing histone demethylation protein 2C isoform X3
probable JmjC domain-containing histone demethylation protein 2C, transcript variant X1
uncharacterized protein LOC124413111 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00049
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
trace amine-associated receptor 9, transcript variant X3
trace amine-associated receptor 9, transcript variant X1
trace amine-associated receptor 9, transcript variant X2
trace amine-associated receptor 9 isoform X3
trace amine-associated receptor 9 isoform X1
trace amine-associated receptor 9 isoform X2
cytoplasmic dynein 2 intermediate chain 1, transcript variant X3
cytoplasmic dynein 2 intermediate chain 1, transcript variant X1
cytoplasmic dynein 2 intermediate chain 1, transcript variant X2
cytoplasmic dynein 2 intermediate chain 1 isoform X1
cytoplasmic dynein 2 intermediate chain 1 isoform X2
cytoplasmic dynein 2 intermediate chain 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
major facilitator superfamily domain-containing protein 6
F-box/WD repeat-containing protein 4-like
transmembrane protein 230, transcript variant X3
transmembrane protein 230, transcript variant X1
transmembrane protein 230, transcript variant X2
LIM domain-binding protein 2, transcript variant X7
LIM domain-binding protein 2, transcript variant X4
LIM domain-binding protein 2, transcript variant X6
LIM domain-binding protein 2, transcript variant X5
LIM domain-binding protein 2, transcript variant X2
LIM domain-binding protein 2, transcript variant X3
LIM domain-binding protein 2, transcript variant X1
AT-rich interactive domain-containing protein 5B-like
phenoloxidase-activating factor 2, transcript variant X4
phenoloxidase-activating factor 2, transcript variant X3
phenoloxidase-activating factor 2, transcript variant X2
phenoloxidase-activating factor 2, transcript variant X1
phenoloxidase-activating factor 2 isoform X4
phenoloxidase-activating factor 2 isoform X3
phenoloxidase-activating factor 2 isoform X2
phenoloxidase-activating factor 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC124413480, transcript variant X3
uncharacterized LOC124413480, transcript variant X2
uncharacterized LOC124413480, transcript variant X1
uncharacterized LOC124413480, transcript variant X4
uncharacterized protein LOC124413480 isoform X3
uncharacterized protein LOC124413480 isoform X2
uncharacterized protein LOC124413480 isoform X1
uncharacterized protein LOC124413480 isoform X4
uncharacterized LOC124413480, transcript variant X5
uncharacterized protein LOC124413480 isoform X5
conserved oligomeric Golgi complex subunit 7
segmentation protein cap'n'collar, transcript variant X5
segmentation protein cap'n'collar, transcript variant X4
segmentation protein cap'n'collar, transcript variant X3
segmentation protein cap'n'collar, transcript variant X2
segmentation protein cap'n'collar, transcript variant X1
segmentation protein cap'n'collar, transcript variant X7
segmentation protein cap'n'collar, transcript variant X6
segmentation protein cap'n'collar, transcript variant X8
segmentation protein cap'n'collar isoform X5
endoplasmic reticulum membrane sensor NFE2L1 isoform X4
endoplasmic reticulum membrane sensor NFE2L1 isoform X3
endoplasmic reticulum membrane sensor NFE2L1 isoform X2
endoplasmic reticulum membrane sensor NFE2L1 isoform X1
segmentation protein cap'n'collar isoform X7
segmentation protein cap'n'collar isoform X6
segmentation protein cap'n'collar isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
endoplasmic reticulum aminopeptidase 2-like, transcript variant X2
endoplasmic reticulum aminopeptidase 2-like, transcript variant X1
endoplasmic reticulum aminopeptidase 2-like, transcript variant X3
endoplasmic reticulum aminopeptidase 2-like isoform X2
endoplasmic reticulum aminopeptidase 2-like isoform X1
endoplasmic reticulum aminopeptidase 2-like isoform X3
sodium- and chloride-dependent glycine transporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21% coverage of the annotated genomic feature by RNAseq alignments
high affinity copper uptake protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
leishmanolysin-like peptidase, transcript variant X1
leishmanolysin-like peptidase, transcript variant X2
leishmanolysin-like peptidase isoform X1
leishmanolysin-like peptidase isoform X2
nuclear factor interleukin-3-regulated protein-like
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
3-oxoacyl-[acyl-carrier-protein] reductase FabG-like
nucleolysin TIAR-like, transcript variant X1
nucleolysin TIAR-like, transcript variant X2
SEC23-interacting protein-like, transcript variant X2
SEC23-interacting protein-like, transcript variant X1
SEC23-interacting protein-like isoform X2
SEC23-interacting protein-like isoform X1
probable ATP-dependent RNA helicase DDX56
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
adhesion G protein-coupled receptor A3, transcript variant X3
adhesion G protein-coupled receptor A3, transcript variant X1
adhesion G protein-coupled receptor A3, transcript variant X4
adhesion G protein-coupled receptor A3, transcript variant X2
adhesion G protein-coupled receptor A3 isoform X1
adhesion G protein-coupled receptor A3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124413571, transcript variant X3
uncharacterized LOC124413571, transcript variant X2
uncharacterized LOC124413571, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
uncharacterized protein LOC124413571 isoform X1
uncharacterized protein LOC124413571 isoform X2
uncharacterized protein LOC124413571 isoform X3
spermine oxidase-like, transcript variant X1
spermine oxidase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 82 samples with support for all annotated introns
translocon-associated protein subunit delta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
serine proteinase stubble-like, transcript variant X2
serine proteinase stubble-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
selenocysteine insertion sequence-binding protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
selenocysteine insertion sequence-binding protein 2, transcript variant X1
selenocysteine insertion sequence-binding protein 2
uncharacterized LOC124413706, transcript variant X1
uncharacterized LOC124413706, transcript variant X2
uncharacterized protein LOC124413706 isoform X1
uncharacterized protein LOC124413706 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
PWWP domain-containing protein 2A-like, transcript variant X1
PWWP domain-containing protein 2A-like, transcript variant X2
PWWP domain-containing protein 2A-like isoform X1
PWWP domain-containing protein 2A-like isoform X2
uncharacterized LOC124413517, transcript variant X1
uncharacterized LOC124413517, transcript variant X2
DALR anticodon-binding domain-containing protein 3, transcript variant X2
DALR anticodon-binding domain-containing protein 3, transcript variant X3
DALR anticodon-binding domain-containing protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
DALR anticodon-binding domain-containing protein 3 isoform X2
DALR anticodon-binding domain-containing protein 3 isoform X1
FHF complex subunit HOOK interacting protein 2A-like, transcript variant X2
FHF complex subunit HOOK interacting protein 2A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
FHF complex subunit HOOK interacting protein 2A-like isoform X2
FHF complex subunit HOOK interacting protein 2A-like isoform X1
hexokinase type 2, transcript variant X2
hexokinase type 2, transcript variant X6
hexokinase type 2, transcript variant X1
hexokinase type 2, transcript variant X4
hexokinase type 2, transcript variant X3
hexokinase type 2, transcript variant X5
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
BRISC complex subunit FAM175B-like, transcript variant X1
BRISC complex subunit FAM175B-like, transcript variant X2
BRISC complex subunit FAM175B-like isoform X1
BRISC complex subunit FAM175B-like isoform X2
Hermansky-Pudlak syndrome 1 protein homolog, transcript variant X3
Hermansky-Pudlak syndrome 1 protein homolog, transcript variant X2
Hermansky-Pudlak syndrome 1 protein homolog, transcript variant X1
uncharacterized protein LOC124413238 isoform X3
Hermansky-Pudlak syndrome 1 protein homolog isoform X2
Hermansky-Pudlak syndrome 1 protein homolog isoform X1
Kv channel-interacting protein 2-like, transcript variant X1
Kv channel-interacting protein 1-like isoform X1
myb-like protein AA, transcript variant X1
myb-like protein AA, transcript variant X2
uncharacterized protein LOC124413049 isoform X1
Kv channel-interacting protein 2-like, transcript variant X2
Kv channel-interacting protein 2-like isoform X2
palmitoyltransferase ZDHHC16B, transcript variant X1
palmitoyltransferase ZDHHC16B, transcript variant X2
palmitoyltransferase ZDHHC16B isoform X1
palmitoyltransferase ZDHHC16B isoform X2
palmitoyltransferase ZDHHC16B, transcript variant X3
palmitoyltransferase ZDHHC16B, transcript variant X4
palmitoyltransferase ZDHHC16B isoform X3
palmitoyltransferase ZDHHC16A isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
GTP-binding protein 2, transcript variant X2
GTP-binding protein 2, transcript variant X1
GTP-binding protein 2, transcript variant X3
protein TAPT1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
protein TAPT1 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
mitochondrial proton/calcium exchanger protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
uncharacterized LOC124413466, transcript variant X3
uncharacterized LOC124413466, transcript variant X1
uncharacterized LOC124413466, transcript variant X2
uncharacterized LOC124413466, transcript variant X4
uncharacterized protein LOC124413466 isoform X1
uncharacterized protein LOC124413466 isoform X2
uncharacterized protein LOC124413466 isoform X3
uncharacterized protein LOC124413466 isoform X4
tyramine receptor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tyramine receptor 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
tyramine/octopamine receptor-like isoform X1
delta-1-pyrroline-5-carboxylate synthase
U4/U6 small nuclear ribonucleoprotein Prp4
dendritic arbor reduction protein 1-like
xaa-Pro aminopeptidase ApepP, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
xaa-Pro aminopeptidase ApepP, transcript variant X3
xaa-Pro aminopeptidase ApepP, transcript variant X4
xaa-Pro aminopeptidase ApepP, transcript variant X1
xaa-Pro aminopeptidase ApepP, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
uncharacterized LOC124413683, transcript variant X2
uncharacterized LOC124413683, transcript variant X1
uncharacterized protein LOC124413683 isoform X2
uncharacterized protein LOC124413683 isoform X1
apoptosis-stimulating of p53 protein 1, transcript variant X7
apoptosis-stimulating of p53 protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
apoptosis-stimulating of p53 protein 1, transcript variant X1
apoptosis-stimulating of p53 protein 1, transcript variant X6
apoptosis-stimulating of p53 protein 1, transcript variant X5
apoptosis-stimulating of p53 protein 1, transcript variant X3
J domain-containing protein DDB_G0295729 isoform X5
apoptosis-stimulating of p53 protein 1 isoform X1
apoptosis-stimulating of p53 protein 1 isoform X4
apoptosis-stimulating of p53 protein 1, transcript variant X4
apoptosis-stimulating of p53 protein 1 isoform X2
apoptosis-stimulating of p53 protein 1 isoform X3
uncharacterized LOC124413685, transcript variant X2
uncharacterized LOC124413685, transcript variant X3
uncharacterized LOC124413685, transcript variant X1
thyroid adenoma-associated protein homolog, transcript variant X1
thyroid adenoma-associated protein homolog, transcript variant X3
thyroid adenoma-associated protein homolog, transcript variant X2
thyroid adenoma-associated protein homolog isoform X1
thyroid adenoma-associated protein homolog isoform X2
thyroid adenoma-associated protein homolog isoform X3
uncharacterized protein CG43867, transcript variant X6
uncharacterized protein CG43867, transcript variant X1
uncharacterized protein CG43867, transcript variant X3
uncharacterized protein CG43867, transcript variant X2
uncharacterized protein CG43867, transcript variant X4
uncharacterized protein CG43867, transcript variant X5
uncharacterized protein CG43867 isoform X6
uncharacterized protein CG43867 isoform X1
uncharacterized protein CG43867 isoform X3
uncharacterized protein CG43867 isoform X2
uncharacterized protein CG43867 isoform X4
uncharacterized protein CG43867 isoform X5
uncharacterized protein CG43867, transcript variant X7
uncharacterized protein CG43867, transcript variant X10
uncharacterized protein CG43867 isoform X7
uncharacterized protein CG43867 isoform X9
uncharacterized protein CG43867, transcript variant X8
uncharacterized protein CG43867, transcript variant X9
uncharacterized protein CG43867 isoform X8
interference hedgehog-like, transcript variant X1
interference hedgehog-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
forkhead box protein N2-like, transcript variant X1
forkhead box protein N2-like, transcript variant X4
forkhead box protein N2-like, transcript variant X2
forkhead box protein N2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
zinc finger FYVE domain-containing protein 1-like, transcript variant X3
zinc finger FYVE domain-containing protein 1-like, transcript variant X2
zinc finger FYVE domain-containing protein 1-like, transcript variant X4
zinc finger FYVE domain-containing protein 1-like, transcript variant X5
zinc finger FYVE domain-containing protein 1-like, transcript variant X1
zinc finger FYVE domain-containing protein 1-like isoform X2
zinc finger FYVE domain-containing protein 1-like isoform X4
zinc finger FYVE domain-containing protein 1-like isoform X1
zinc finger FYVE domain-containing protein 1-like isoform X3
GTP-binding protein Rheb homolog, transcript variant X1
GTP-binding protein Rheb homolog, transcript variant X2
GTP-binding protein Rheb homolog isoform X1
GTP-binding protein Rheb homolog isoform X2
LOW QUALITY PROTEIN: ubiquitin carboxyl-terminal hydrolase 8
ralA-binding protein 1, transcript variant X4
ralA-binding protein 1, transcript variant X5
ralA-binding protein 1, transcript variant X2
ralA-binding protein 1, transcript variant X3
ralA-binding protein 1, transcript variant X1
cell growth-regulating nucleolar protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 83 samples with support for all annotated introns
EP300-interacting inhibitor of differentiation 3
U4/U6 small nuclear ribonucleoprotein Prp3