Vespula pensylvanica isolate Volc-1 chromosome 11, ASM1446617v1, whole genome shotgun sequence.
Vespula pensylvanica (western yellowjacket)
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Apocrita; Aculeata; Vespoidea; Vespidae; Vespinae; Vespula.
High-Quality Assemblies for Three Invasive Social Wasps from the Vespula Genus
Publication Status: Available-Online prior to print
REFSEQ INFORMATION: The reference sequence is identical to\nCM025346.1.\nAssembly name: ASM1446617v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the University of Otago on\n2020/09/09. The original whole-genome shotgun project has the\naccession JACSDY000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: University of Otago\nAssembly Date :: 03-JUL-2020\nAssembly Method :: meraculous v. 2.2.6\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 644x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Vespula pensylvanica Annotation\n Release 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##
Derived by automated computational analysis using gene prediction method: Gnomon.
transcription initiation factor TFIID subunit 4, transcript variant X6
COORDINATES: polyA evidence [ECO:0006239]
transcription initiation factor TFIID subunit 4, transcript variant X5
transcription initiation factor TFIID subunit 4, transcript variant X3
transcription initiation factor TFIID subunit 4, transcript variant X4
transcription initiation factor TFIID subunit 4, transcript variant X2
transcription initiation factor TFIID subunit 4, transcript variant X1
transcription initiation factor TFIID subunit 4 isoform X6
transcription initiation factor TFIID subunit 4 isoform X5
transcription initiation factor TFIID subunit 4 isoform X3
transcription initiation factor TFIID subunit 4 isoform X4
transcription initiation factor TFIID subunit 4 isoform X2
transcription initiation factor TFIID subunit 4 isoform X1
peptidoglycan-recognition protein LC-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, including 38 samples with support for all annotated introns
transcription elongation factor B polypeptide 3
actin-related protein 8, transcript variant X2
actin-related protein 8, transcript variant X1
actin-related protein 8, transcript variant X3
uncharacterized LOC122633193, 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 22 samples with support for all annotated introns
uncharacterized LOC122633193, 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
uncharacterized protein LOC122633193 isoform X1
uncharacterized protein LOC122633193 isoform X2
pre-mRNA-splicing factor CWC22 homolog, 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 3 samples with support for all annotated introns
pre-mRNA-splicing factor CWC22 homolog, transcript variant X2
pre-mRNA-splicing factor CWC22 homolog isoform X1
pre-mRNA-splicing factor CWC22 homolog isoform 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 30 samples with support for all annotated introns
uncharacterized LOC122633195, transcript variant X1
uncharacterized LOC122633195, 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 3 samples with support for all annotated introns
uncharacterized LOC122633195, 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 5 samples with support for all annotated introns
uncharacterized LOC122633196, 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 2 samples with support for all annotated introns
uncharacterized LOC122633196, transcript variant X1
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
uncharacterized LOC122633196, 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
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 46 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 42 samples with support for all annotated introns
probable enoyl-CoA hydratase, mitochondrial
mediator of RNA polymerase II transcription subunit 15
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
myotubularin-related protein DDB_G0290005-like
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
leucine-rich repeats and immunoglobulin-like domains protein 3, transcript variant X2
leucine-rich repeats and immunoglobulin-like domains protein 3, transcript variant X1
leucine-rich repeats and immunoglobulin-like domains protein 3 isoform X1
leucine-rich repeats and immunoglobulin-like domains protein 3 isoform X2
histone lysine demethylase PHF8-like, 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 13 samples with support for all annotated introns
histone lysine demethylase PHF8-like, 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 13 samples with support for all annotated introns
histone lysine demethylase PHF8-like, 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 35 samples with support for all annotated introns
histone lysine demethylase PHF8-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 34 samples with support for all annotated introns
histone lysine demethylase PHF8-like isoform X3
histone lysine demethylase PHF8-like isoform X2
histone lysine demethylase PHF8-like isoform X4
histone lysine demethylase PHF8-like isoform X1
polynucleotide 5'-hydroxyl-kinase NOL9, transcript variant X1
polynucleotide 5'-hydroxyl-kinase NOL9, transcript variant X2
polynucleotide 5'-hydroxyl-kinase NOL9 isoform X1
polynucleotide 5'-hydroxyl-kinase NOL9 isoform X2
DNA (cytosine-5)-methyltransferase 3C-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 2 samples with support for all annotated introns
DNA (cytosine-5)-methyltransferase 3C-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 9 samples with support for all annotated introns
DNA (cytosine-5)-methyltransferase 3C-like, transcript variant X1
DNA (cytosine-5)-methyltransferase 3C-like isoform X3
DNA (cytosine-5)-methyltransferase 3B-like isoform X2
DNA (cytosine-5)-methyltransferase 3B-like isoform X1
putative RNA-binding protein Luc7-like 2, transcript variant X1
putative RNA-binding protein Luc7-like 2 isoform X1
putative RNA-binding protein Luc7-like 2, transcript variant X4
putative RNA-binding protein Luc7-like 2, transcript variant X2
putative RNA-binding protein Luc7-like 2, transcript variant X3
putative RNA-binding protein Luc7-like 2, transcript variant X5
putative RNA-binding protein Luc7-like 2 isoform X2
putative RNA-binding protein Luc7-like 2 isoform X3
SHC-transforming protein 1, transcript variant X2
SHC-transforming protein 1, transcript variant X1
replication factor C subunit 2, transcript variant X1
replication factor C subunit 2, transcript variant X2
replication factor C subunit 2 isoform X1
replication factor C subunit 2 isoform X2
leucine-rich repeat flightless-interacting protein 2, transcript variant X3
leucine-rich repeat flightless-interacting protein 2, transcript variant X4
leucine-rich repeat flightless-interacting protein 2, transcript variant X1
leucine-rich repeat flightless-interacting protein 2, transcript variant X2
leucine-rich repeat flightless-interacting protein 2, transcript variant X5
leucine-rich repeat flightless-interacting protein 2 isoform X1
leucine-rich repeat flightless-interacting protein 2 isoform X2
leucine-rich repeat flightless-interacting protein 2 isoform X3
uncharacterized LOC122633092, transcript variant X2
uncharacterized LOC122633092, transcript variant X1
monocarboxylate transporter 12, transcript variant X3
monocarboxylate transporter 12, transcript variant X1
monocarboxylate transporter 12, transcript variant X2
glutamate [NMDA] receptor subunit 1, 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 18 samples with support for all annotated introns
glutamate [NMDA] receptor subunit 1, 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 19 samples with support for all annotated introns
glutamate [NMDA] receptor subunit 1, transcript variant X5
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
glutamate [NMDA] receptor subunit 1, transcript variant X6
glutamate [NMDA] receptor subunit 1, transcript variant X2
glutamate [NMDA] receptor subunit 1, transcript variant X1
glutamate [NMDA] receptor subunit 1 isoform X1
glutamate [NMDA] receptor subunit 1 isoform X2
glutamate [NMDA] receptor subunit 1 isoform X3
glutamate [NMDA] receptor subunit 1 isoform 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 36 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 38 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 38 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 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 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
myb-like protein X, transcript variant X5
myb-like protein X, transcript variant X4
myb-like protein X, transcript variant X1
myb-like protein X, transcript variant X2
myb-like protein X, transcript variant X3
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X3
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X12
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X7
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X6
guanine nucleotide-binding protein G(q) subunit alpha isoform X6
guanine nucleotide-binding protein G(q) subunit alpha isoform X3
guanine nucleotide-binding protein G(q) subunit alpha isoform X7
guanine nucleotide-binding protein G(q) subunit alpha isoform X12
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X1
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X13
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X2
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X11
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X4
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X9
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X10
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X5
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X8
guanine nucleotide-binding protein G(q) subunit alpha isoform X11
guanine nucleotide-binding protein G(q) subunit alpha isoform X9
guanine nucleotide-binding protein G(q) subunit alpha isoform X13
guanine nucleotide-binding protein G(q) subunit alpha isoform X5
guanine nucleotide-binding protein G(q) subunit alpha isoform X4
guanine nucleotide-binding protein G(q) subunit alpha isoform X1
uncharacterized LOC122633087, 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 19 samples with support for all annotated introns
uncharacterized LOC122633087, 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 21 samples with support for all annotated introns
uncharacterized LOC122633087, 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 10 samples with support for all annotated introns
uncharacterized LOC122633087, transcript variant X5
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 27 samples with support for all annotated introns
uncharacterized LOC122633087, transcript variant X1
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
uncharacterized protein LOC122633087 isoform X2
uncharacterized protein LOC122633087 isoform X4
uncharacterized protein LOC122633087 isoform X1
uncharacterized protein LOC122633087 isoform X3
myc box-dependent-interacting protein 1, transcript variant X4
myc box-dependent-interacting protein 1, transcript variant X3
myc box-dependent-interacting protein 1, transcript variant X1
myc box-dependent-interacting protein 1, transcript variant X2
myc box-dependent-interacting protein 1 isoform X4
myc box-dependent-interacting protein 1 isoform X3
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X3
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X1
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X4
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X2
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X3
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X1
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X4
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X2
uncharacterized LOC122633014, transcript variant X1
uncharacterized LOC122633014, transcript variant X3
uncharacterized LOC122633014, transcript variant X2
uncharacterized protein LOC122633014 isoform X1
uncharacterized protein LOC122633014 isoform X2
heparan sulfate glucosamine 3-O-sulfotransferase 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 13 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 1-like, 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 30 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 1-like
probable protein phosphatase CG10417, transcript variant X1
probable protein phosphatase CG10417, transcript variant X2
probable protein phosphatase CG10417, transcript variant X3
probable protein phosphatase CG10417 isoform X1
probable protein phosphatase CG10417 isoform X2
intraflagellar transport protein 20 homolog
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 39 samples with support for all annotated introns
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3, transcript variant X1
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3, transcript variant X2
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 isoform X1
BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 isoform X2
elongation of very long chain fatty acids protein 6
nuclear envelope phosphatase-regulatory subunit 1, transcript variant X1
nuclear envelope phosphatase-regulatory subunit 1, transcript variant X3
nuclear envelope phosphatase-regulatory subunit 1, transcript variant X2
nuclear envelope phosphatase-regulatory subunit 1 isoform X2
nuclear envelope phosphatase-regulatory subunit 1 isoform X1
nuclear envelope phosphatase-regulatory subunit 1 isoform X3
regulation of nuclear pre-mRNA domain-containing protein 1B
85/88 kDa calcium-independent phospholipase A2, 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 11 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2, 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 40 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2
sex-determining region Y protein-like, transcript variant 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 8 samples with support for all annotated introns
sex-determining region Y protein-like, transcript variant X1
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 17 samples with support for all annotated introns
transcription factor Sox-10-like, transcript variant X1
transcription factor Sox-10-like, transcript variant X3
transcription factor Sox-10-like, transcript variant X2
transcription factor Sox-10-like, transcript variant X4
transcription factor Sox-10-like isoform X1
transcription factor Sox-10-like isoform X2
transcription factor Sox-10-like isoform X3
zinc transporter ZIP11, transcript variant X4
uncharacterized Golgi apparatus membrane protein-like protein CG5021, transcript variant X5
zinc transporter ZIP11, 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 5 samples with support for all annotated introns
zinc transporter ZIP11, transcript variant X6
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 9 samples with support for all annotated introns
zinc transporter ZIP11, 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 12 samples with support for all annotated introns
zinc transporter ZIP11, transcript variant X5
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 12 samples with support for all annotated introns
zinc transporter ZIP11, transcript variant X3
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, including 40 samples with support for all annotated introns
uncharacterized Golgi apparatus membrane protein-like protein CG5021, transcript variant X2
uncharacterized Golgi apparatus membrane protein-like protein CG5021, transcript variant X1
uncharacterized Golgi apparatus membrane protein-like protein CG5021, transcript variant X4
uncharacterized Golgi apparatus membrane protein-like protein CG5021 isoform X1
uncharacterized Golgi apparatus membrane protein-like protein CG5021 isoform X2
uncharacterized Golgi apparatus membrane protein-like protein CG5021, transcript variant X3
uncharacterized Golgi apparatus membrane protein-like protein CG5021 isoform X3
tyrosine-protein phosphatase Lar, transcript variant X2
tyrosine-protein phosphatase Lar, transcript variant X3
tyrosine-protein phosphatase Lar, transcript variant X7
tyrosine-protein phosphatase Lar, transcript variant X6
tyrosine-protein phosphatase Lar, transcript variant X9
tyrosine-protein phosphatase Lar, transcript variant X1
tyrosine-protein phosphatase Lar, transcript variant X14
tyrosine-protein phosphatase Lar, transcript variant X12
tyrosine-protein phosphatase Lar, transcript variant X10
tyrosine-protein phosphatase Lar, transcript variant X8
tyrosine-protein phosphatase Lar, transcript variant X11
tyrosine-protein phosphatase Lar, transcript variant X13
tyrosine-protein phosphatase Lar, transcript variant X17
tyrosine-protein phosphatase Lar, transcript variant X18
tyrosine-protein phosphatase Lar, transcript variant X16
tyrosine-protein phosphatase Lar, transcript variant X15
tyrosine-protein phosphatase Lar, transcript variant X5
tyrosine-protein phosphatase Lar, transcript variant X4
tyrosine-protein phosphatase Lar isoform X10
tyrosine-protein phosphatase Lar isoform X2
tyrosine-protein phosphatase Lar isoform X9
tyrosine-protein phosphatase Lar isoform X14
tyrosine-protein phosphatase Lar isoform X8
tyrosine-protein phosphatase Lar isoform X7
tyrosine-protein phosphatase Lar isoform X6
tyrosine-protein phosphatase Lar isoform X13
tyrosine-protein phosphatase Lar isoform X12
tyrosine-protein phosphatase Lar isoform X11
tyrosine-protein phosphatase Lar isoform X5
tyrosine-protein phosphatase Lar isoform X4
tyrosine-protein phosphatase Lar isoform X3
tyrosine-protein phosphatase Lar isoform X1
tyrosine-protein phosphatase Lar, transcript variant X19
tyrosine-protein phosphatase Lar isoform X15
uncharacterized LOC122633003, 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 protein LOC122633003 isoform X2
uncharacterized LOC122633003, 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
uncharacterized protein LOC122633003 isoform X1
uncharacterized LOC122633003, transcript variant X3
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 19 samples with support for all annotated introns
uncharacterized protein LOC122633003 isoform X3
uncharacterized LOC122633057, transcript variant X1
uncharacterized LOC122633057, transcript variant X2
uncharacterized protein LOC122633057 isoform X1
uncharacterized protein LOC122633057 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 21 samples with support for all annotated introns
serine-rich adhesin for platelets-like, transcript variant X2
serine-rich adhesin for platelets-like, transcript variant X1
serine-rich adhesin for platelets-like isoform X1
serine-rich adhesin for platelets-like isoform X2
serine/threonine-protein kinase meng-po, 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 39 samples with support for all annotated introns
serine/threonine-protein kinase meng-po, 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 24 samples with support for all annotated introns
ciliogenesis and planar polarity effector 2-like, transcript variant X1
ciliogenesis and planar polarity effector 2-like, transcript variant X2
ciliogenesis and planar polarity effector 2-like isoform X1
ciliogenesis and planar polarity effector 2-like isoform X2
heterogeneous nuclear ribonucleoprotein U-like protein 1, transcript variant X2
heterogeneous nuclear ribonucleoprotein U-like protein 1, transcript variant X1
heterogeneous nuclear ribonucleoprotein U-like protein 1, 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 24 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein U-like protein 1, 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 28 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein U-like protein 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 40 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein U-like protein 1, transcript variant X5
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 8 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein U-like protein 1, transcript variant X8
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
heterogeneous nuclear ribonucleoprotein U-like protein 1, transcript variant X3
heterogeneous nuclear ribonucleoprotein U-like protein 1, transcript variant X7
heterogeneous nuclear ribonucleoprotein U-like protein 1 isoform X1
heterogeneous nuclear ribonucleoprotein U-like protein 1 isoform X2
heterogeneous nuclear ribonucleoprotein U-like protein 1 isoform X3
histone-lysine N-methyltransferase ash1, transcript variant X5
histone-lysine N-methyltransferase ash1, transcript variant X3
histone-lysine N-methyltransferase ash1, transcript variant X4
histone-lysine N-methyltransferase ash1, transcript variant X6
histone-lysine N-methyltransferase ash1, transcript variant X1
histone-lysine N-methyltransferase ash1, transcript variant X2
histone-lysine N-methyltransferase ash1 isoform X2
histone-lysine N-methyltransferase ash1 isoform X1
protein enabled-like, transcript variant X1
protein enabled-like, transcript variant X2
protein enabled-like, transcript variant X3
uncharacterized LOC122633169, transcript variant X4
uncharacterized LOC122633169, transcript variant X1
uncharacterized LOC122633169, transcript variant X2
uncharacterized LOC122633169, transcript variant X5
uncharacterized LOC122633169, transcript variant X3
uncharacterized LOC122633169, transcript variant X7
uncharacterized LOC122633169, transcript variant X6
uncharacterized LOC122633169, transcript variant X9
uncharacterized LOC122633169, transcript variant X8
uncharacterized LOC122633169, transcript variant X10
uncharacterized protein LOC122633169 isoform X1
uncharacterized protein LOC122633169 isoform X2
uncharacterized protein LOC122633169 isoform X5
uncharacterized protein LOC122633169 isoform X3
uncharacterized protein LOC122633169 isoform X7
uncharacterized protein LOC122633169 isoform X6
uncharacterized protein LOC122633169 isoform X9
uncharacterized protein LOC122633169 isoform X8
uncharacterized protein LOC122633169 isoform X10
uncharacterized protein LOC122633169 isoform X4
SKI/DACH domain-containing protein 1-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
cuticle protein 65-like, transcript variant X1
cuticle protein 65-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
cuticle protein 70, isoforms A and B-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
uncharacterized LOC122632874, transcript variant X1
uncharacterized LOC122632874, transcript variant X2
uncharacterized protein LOC122632874 isoform X1
uncharacterized protein LOC122632874 isoform X2
uncharacterized LOC122632877, transcript variant X1
uncharacterized LOC122632877, transcript variant X2
uncharacterized protein LOC122632877 isoform X1
uncharacterized protein LOC122632877 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 17 samples with support for all annotated introns
uncharacterized LOC122632875, transcript variant X4
uncharacterized LOC122632875, transcript variant X1
uncharacterized LOC122632875, transcript variant X2
uncharacterized LOC122632875, transcript variant X3
uncharacterized protein LOC122632875 isoform X2
uncharacterized protein LOC122632875 isoform X1
uncharacterized protein LOC122632875 isoform X3
transfer RNA isoleucine (anticodon UAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
TATA element modulatory factor-like, transcript variant X3
TATA element modulatory factor-like, transcript variant X2
TATA element modulatory factor-like, transcript variant X4
TATA element modulatory factor-like, transcript variant X1
TATA element modulatory factor-like, transcript variant X5
TATA element modulatory factor-like isoform X1
TATA element modulatory factor-like isoform X3
TATA element modulatory factor-like isoform X2
TATA element modulatory factor-like isoform X4
TATA element modulatory factor-like isoform X5
serine/threonine-protein kinase SMG1, transcript variant X1
serine/threonine-protein kinase SMG1, transcript variant X2
ATP synthase subunit d, mitochondrial-like
uncharacterized LOC122633209, 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
uncharacterized LOC122633209, transcript variant X2
uncharacterized protein LOC122633209 isoform X1
uncharacterized protein LOC122633209 isoform X2
cytochrome b-c1 complex subunit 2, mitochondrial
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 LOC122633152, transcript variant X3
uncharacterized LOC122633152, transcript variant X4
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 15 samples with support for all annotated introns
uncharacterized LOC122633152, 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 31 samples with support for all annotated introns
uncharacterized LOC122633152, 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 16 samples with support for all annotated introns
uncharacterized protein LOC122633152 isoform X3
uncharacterized protein LOC122633152 isoform X2
uncharacterized protein LOC122633152 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 17 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 10, transcript variant X2
zinc finger CCHC domain-containing protein 10, transcript variant X1
zinc finger CCHC domain-containing protein 10 isoform X1
zinc finger CCHC domain-containing protein 10 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat protein soc-2 homolog
mpv17-like protein, transcript variant X3
mpv17-like protein, transcript variant X1
mpv17-like protein, transcript variant X2
transcription factor E2F4-like, transcript variant X1
transcription factor E2F4-like, transcript variant X2
transcription factor E2F4-like, transcript variant X3
transcription factor E2F4-like isoform X1
transcription factor E2F4-like isoform X2
transcription factor E2F4-like isoform X3
transcription initiation factor TFIID subunit 2, transcript variant X2
transcription initiation factor TFIID subunit 2, transcript variant X1
transcription initiation factor TFIID subunit 2 isoform X2
transcription initiation factor TFIID subunit 2 isoform X1
exosome complex component CSL4, transcript variant X1
exosome complex component CSL4, transcript variant X2
kinesin-like protein KIF19, transcript variant X1
kinesin-like protein KIF19, transcript variant X3
kinesin-like protein KIF19, transcript variant X2
uncharacterized LOC122632826, 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 3 samples with support for all annotated introns
uncharacterized LOC122632826, transcript variant X1
peptide methionine sulfoxide reductase, transcript variant X1
peptide methionine sulfoxide reductase isoform X1
peptide methionine sulfoxide reductase, transcript variant X3
peptide methionine sulfoxide reductase, transcript variant X2
peptide methionine sulfoxide reductase, transcript variant X4
peptide methionine sulfoxide reductase isoform X2
protein phosphatase 1 regulatory subunit 16A, transcript variant X4
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
protein phosphatase 1 regulatory subunit 16A, transcript variant X5
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
protein phosphatase 1 regulatory subunit 16A, transcript variant X8
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
protein phosphatase 1 regulatory subunit 16A, transcript variant X10
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
protein phosphatase 1 regulatory subunit 16A, 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 20 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 16A, transcript variant X2
protein phosphatase 1 regulatory subunit 16A, transcript variant X9
protein phosphatase 1 regulatory subunit 16A, 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 33 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 16A, transcript variant X7
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 4 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 16A, transcript variant X6
protein phosphatase 1 regulatory subunit 16A isoform X8
protein phosphatase 1 regulatory subunit 16A isoform X4
protein phosphatase 1 regulatory subunit 16A isoform X3
protein phosphatase 1 regulatory subunit 16A isoform X2
protein phosphatase 1 regulatory subunit 16A isoform X1
protein phosphatase 1 regulatory subunit 16A isoform X7
protein phosphatase 1 regulatory subunit 16A isoform X6
protein phosphatase 1 regulatory subunit 16A isoform X5
protein phosphatase 1 regulatory subunit 16A isoform X9
protein phosphatase 1 regulatory subunit 16A, transcript variant X11
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
protein phosphatase 1 regulatory subunit 16A isoform X10
transmembrane protein 42-like, transcript variant X1
transmembrane protein 42-like isoform X1
transmembrane protein 42-like, transcript variant X2
transmembrane protein 42-like isoform X2
dual specificity protein phosphatase 15, 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 12 samples with support for all annotated introns
dual specificity protein phosphatase 15, 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 18 samples with support for all annotated introns
dual specificity protein phosphatase 15, 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 10 samples with support for all annotated introns
ER membrane protein complex subunit 8/9 homolog
uncharacterized LOC122632827, transcript variant X2
trichohyalin-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 2 samples with support for all annotated introns
trichohyalin-like, transcript variant X3
trichohyalin-like, transcript variant X2
trichohyalin-like, transcript variant X4
trichohyalin-like, transcript variant X5
uncharacterized LOC122632827, transcript variant X1
uncharacterized LOC122632827, transcript variant X3
uncharacterized LOC122632827, transcript variant X4
uncharacterized protein LOC122632827 isoform X2
uncharacterized protein LOC122632827 isoform X1
uncharacterized protein LOC122632827 isoform X3
dehydrodolichyl diphosphate synthase complex subunit DHDDS, transcript variant X2
dehydrodolichyl diphosphate synthase complex subunit DHDDS, transcript variant X1
dehydrodolichyl diphosphate synthase complex subunit DHDDS
uncharacterized LOC122632823, transcript variant X1
uncharacterized LOC122632823, transcript variant X2
uncharacterized protein LOC122632823 isoform X1
uncharacterized protein LOC122632823 isoform X2
probable cytochrome P450 301a1, mitochondrial, transcript variant X6
probable cytochrome P450 301a1, mitochondrial, transcript variant X4
probable cytochrome P450 301a1, mitochondrial, transcript variant X2
probable cytochrome P450 301a1, mitochondrial, transcript variant X3
probable cytochrome P450 301a1, mitochondrial, transcript variant X1
probable cytochrome P450 301a1, mitochondrial, transcript variant X5
probable cytochrome P450 301a1, mitochondrial isoform X1
probable cytochrome P450 301a1, mitochondrial isoform X2
probable cytochrome P450 301a1, mitochondrial isoform X3
uncharacterized LOC122632814, transcript variant X2
uncharacterized LOC122632814, transcript variant X3
uncharacterized protein LOC122632814 isoform X2
uncharacterized LOC122632814, transcript variant X4
uncharacterized LOC122632814, transcript variant X1
uncharacterized protein LOC122632814 isoform X3
uncharacterized protein LOC122632814 isoform X1
trafficking protein particle complex subunit 10, 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
trafficking protein particle complex subunit 10, transcript variant X1
trafficking protein particle complex subunit 10 isoform X2
trafficking protein particle complex subunit 10 isoform X1
H/ACA ribonucleoprotein complex subunit 3
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
zinc finger protein 628-like, 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 12 samples with support for all annotated introns
zinc finger protein 628-like, transcript variant 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 1 sample with support for all annotated introns
zinc finger protein 628-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 2 samples with support for all annotated introns
uncharacterized LOC122632833, transcript variant X2
uncharacterized LOC122632833, transcript variant X1
BTB/POZ domain-containing protein KCTD1, 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 21 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD1, transcript variant X2
discoidin domain-containing receptor 2-like, transcript variant X3
discoidin domain-containing receptor 2-like, transcript variant X2
discoidin domain-containing receptor 2-like, transcript variant X1
discoidin domain-containing receptor 2-like isoform X2
discoidin domain-containing receptor 2-like isoform X1
discoidin domain-containing receptor 2-like isoform X3
uncharacterized LOC122633138, transcript variant X3
uncharacterized LOC122633138, transcript variant X2
uncharacterized LOC122633138, transcript variant X1
uncharacterized LOC122633138, transcript variant X4
uncharacterized LOC122633138, transcript variant X5
discoidin domain-containing receptor 2, 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 1 sample with support for all annotated introns
discoidin domain-containing receptor 2, 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 4 samples with support for all annotated introns
discoidin domain-containing receptor 2, transcript variant X3
discoidin domain-containing receptor 2, 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 3 samples with support for all annotated introns
discoidin domain-containing receptor 2 isoform X1
discoidin domain-containing receptor 2, transcript variant X6
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 8 samples with support for all annotated introns
discoidin domain-containing receptor 2, transcript variant X5
discoidin domain-containing receptor 2 isoform 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 9 samples with support for all annotated introns
discoidin domain-containing receptor 2-like, transcript variant X4
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 10 samples with support for all annotated introns
discoidin domain-containing receptor 2-like, transcript variant X5
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 8 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 15 samples with support for all annotated introns
discoidin domain-containing receptor 2-like, transcript variant X6
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 20 samples with support for all annotated introns
discoidin domain-containing receptor 2-like
discoidin domain-containing receptor tyrosine kinase B-like
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
geranylgeranyl transferase type-2 subunit beta, transcript variant X2
geranylgeranyl transferase type-2 subunit beta, transcript variant X1
geranylgeranyl transferase type-2 subunit beta, transcript variant X3
geranylgeranyl transferase type-2 subunit beta isoform X1
geranylgeranyl transferase type-2 subunit beta isoform X2
WD repeat-containing protein 43, transcript variant X1
WD repeat-containing protein 43, transcript variant X2
iron-sulfur cluster assembly 1 homolog, mitochondrial
coiled-coil domain-containing protein 40, transcript variant X1
coiled-coil domain-containing protein 40, transcript variant X2
coiled-coil domain-containing protein 40 isoform X1
coiled-coil domain-containing protein 40 isoform X2
thyroid receptor-interacting protein 6, transcript variant X3
thyroid receptor-interacting protein 6, transcript variant X1
thyroid receptor-interacting protein 6, 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 1 sample with support for all annotated introns
uncharacterized LOC122632958, transcript variant X3
uncharacterized LOC122632958, transcript variant X2
uncharacterized LOC122632958, transcript variant X1
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
sodium-coupled monocarboxylate transporter 2-like, transcript variant X6
sodium-coupled monocarboxylate transporter 2-like, transcript variant X5
sodium-coupled monocarboxylate transporter 2-like, transcript variant X4
sodium-coupled monocarboxylate transporter 2-like, transcript variant X3
sodium-coupled monocarboxylate transporter 2-like, transcript variant X7
sodium-coupled monocarboxylate transporter 2-like, transcript variant X1
sodium-coupled monocarboxylate transporter 2-like, transcript variant X2
sodium-coupled monocarboxylate transporter 2-like isoform X2
sodium-coupled monocarboxylate transporter 2-like isoform X1
sodium-coupled monocarboxylate transporter 2-like isoform X3
endoplasmic reticulum transmembrane helix translocase
blood vessel epicardial substance-like, transcript variant X2
blood vessel epicardial substance-like, transcript variant X3
blood vessel epicardial substance-like, transcript variant X4
blood vessel epicardial substance-like, transcript variant X1
blood vessel epicardial substance-like isoform X1
blood vessel epicardial substance-like isoform X2
uncharacterized LOC122632790, transcript variant X1
uncharacterized LOC122632790, transcript variant X2
uncharacterized protein LOC122632790 isoform X2
uncharacterized protein LOC122632790 isoform X1
protein vestigial, transcript variant X4
protein vestigial, transcript variant X3
protein vestigial, transcript variant X2
protein vestigial, transcript variant X1
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
HIV Tat-specific factor 1 homolog, transcript variant X2
HIV Tat-specific factor 1 homolog, transcript variant X1
X-linked retinitis pigmentosa GTPase regulator
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
peptidylglycine alpha-hydroxylating monooxygenase
uncharacterized LOC122633112, transcript variant X3
uncharacterized LOC122633112, transcript variant X1
uncharacterized LOC122633112, transcript variant X2
uncharacterized protein LOC122633112 isoform X1
uncharacterized protein LOC122633112 isoform X2
UBX domain-containing protein 1, transcript variant X1
UBX domain-containing protein 1, transcript variant X2
UBX domain-containing protein 1 isoform X1
UBX domain-containing protein 1 isoform X2
uncharacterized protein DDB_G0283697-like
uncharacterized LOC122633126, transcript variant X1
uncharacterized LOC122633126, transcript variant X2
protein croquemort-like, transcript variant X1
protein croquemort-like, transcript variant X2
protein borderless, transcript variant X2
protein borderless, transcript variant X1
polyphosphoinositide phosphatase, 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 17 samples with support for all annotated introns
polyphosphoinositide phosphatase, 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 19 samples with support for all annotated introns
polyphosphoinositide phosphatase, transcript variant 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 31 samples with support for all annotated introns
polyphosphoinositide phosphatase isoform X3
polyphosphoinositide phosphatase isoform X2
polyphosphoinositide phosphatase isoform X1
uncharacterized LOC122633200, transcript variant X4
uncharacterized LOC122633200, transcript variant X1
uncharacterized LOC122633200, transcript variant X2
uncharacterized LOC122633200, transcript variant X3
uncharacterized protein LOC122633200 isoform X1
uncharacterized protein LOC122633200 isoform X2
gamma-aminobutyric acid type B receptor subunit 2
excitatory amino acid transporter, transcript variant X1
excitatory amino acid transporter, transcript variant X2
excitatory amino acid transporter, transcript variant X3
excitatory amino acid transporter isoform X1
excitatory amino acid transporter isoform X2
uncharacterized LOC122632886, 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 6 samples with support for all annotated introns
uncharacterized LOC122632886, transcript variant X3
uncharacterized LOC122632886, transcript variant X1
ATP-binding cassette sub-family G member 4
ATP-binding cassette sub-family G member 1, transcript variant X6
ATP-binding cassette sub-family G member 1, transcript variant X7
ATP-binding cassette sub-family G member 1, transcript variant X3
ATP-binding cassette sub-family G member 1, transcript variant X4
ATP-binding cassette sub-family G member 1, transcript variant X8
ATP-binding cassette sub-family G member 1, transcript variant X5
ATP-binding cassette sub-family G member 1, transcript variant X1
ATP-binding cassette sub-family G member 1 isoform X2
ATP-binding cassette sub-family G member 1, transcript variant X2
ATP-binding cassette sub-family G member 1 isoform X1
ATP-binding cassette sub-family G member 1-like, 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 34 samples with support for all annotated introns
ATP-binding cassette sub-family G member 1-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 32 samples with support for all annotated introns
ATP-binding cassette sub-family G member 1-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 22 samples with support for all annotated introns
ATP-binding cassette sub-family G member 1-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 29 samples with support for all annotated introns
PRELI domain-containing protein 1, mitochondrial
uncharacterized LOC122633041, transcript variant X1
uncharacterized LOC122633041, transcript variant X3
uncharacterized protein LOC122633041 isoform X1
uncharacterized protein LOC122633041 isoform X2
uncharacterized LOC122633041, 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 30 samples with support for all annotated introns
uncharacterized LOC122632944, transcript variant X3
uncharacterized protein LOC122632944 isoform X3
uncharacterized LOC122632944, transcript variant X1
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 LOC122632944, 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 13 samples with support for all annotated introns
uncharacterized protein LOC122632944 isoform X1
uncharacterized protein LOC122632944 isoform X2
small glutamine-rich tetratricopeptide repeat-containing protein alpha, transcript variant X1
small glutamine-rich tetratricopeptide repeat-containing protein alpha, transcript variant X4
small glutamine-rich tetratricopeptide repeat-containing protein alpha, transcript variant X2
small glutamine-rich tetratricopeptide repeat-containing protein alpha, transcript variant X3
small glutamine-rich tetratricopeptide repeat-containing protein alpha isoform X1
small glutamine-rich tetratricopeptide repeat-containing protein alpha isoform X2
ATP-binding cassette sub-family D member 3, transcript variant X2
ATP-binding cassette sub-family D member 3, transcript variant X1
ATP-binding cassette sub-family D member 3
uncharacterized LOC122632912, transcript variant X1
uncharacterized LOC122632912, transcript variant X2
uncharacterized protein LOC122632912 isoform X1
uncharacterized protein LOC122632912 isoform X2
endonuclease III-like protein 1, transcript variant X1
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 24 samples with support for all annotated introns
endonuclease III-like protein 1, 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 48 samples with support for all annotated introns
endonuclease III-like protein 1 isoform X1
endonuclease III-like protein 1 isoform X2
nucleolar protein 12, transcript variant X1
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 29 samples with support for all annotated introns
nucleolar protein 12, 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 20 samples with support for all annotated introns
ras-like GTP-binding protein Rho1, transcript variant X5
ras-like GTP-binding protein Rho1, transcript variant X2
ras-like GTP-binding protein Rho1, transcript variant X4
ras-like GTP-binding protein Rho1, transcript variant X3
ras-like GTP-binding protein Rho1 isoform X3
ras-like GTP-binding protein Rho1, transcript variant X1
ras-like GTP-binding protein Rho1, transcript variant X6
ras-like GTP-binding protein Rho1 isoform X1
ras-like GTP-binding protein Rho1 isoform X2
ras-like GTP-binding protein Rho1 isoform X4
UDP-N-acetylglucosamine transferase subunit ALG13 homolog
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial, transcript variant X1
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial, transcript variant X2
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial isoform X2
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial isoform X1
lysophospholipase D GDPD1-like, transcript variant X2
lysophospholipase D GDPD1-like, transcript variant X1
centromere-associated protein E, transcript variant X2
centromere-associated protein E, transcript variant X1
vacuolar protein sorting-associated protein 13, 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 14 samples with support for all annotated introns
vacuolar protein sorting-associated protein 13, 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 18 samples with support for all annotated introns
vacuolar protein sorting-associated protein 13, 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 20 samples with support for all annotated introns
vacuolar protein sorting-associated protein 13, transcript variant X4
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 17 samples with support for all annotated introns
vacuolar protein sorting-associated protein 13 isoform X1
vacuolar protein sorting-associated protein 13 isoform X2
vacuolar protein sorting-associated protein 13 isoform X3
vacuolar protein sorting-associated protein 13 isoform X4
protein lifeguard 3-like, transcript variant X1
protein lifeguard 3-like, transcript variant X2
galactokinase-like, transcript variant X1
galactokinase-like, transcript variant X2
sodium-independent sulfate anion transporter-like, transcript variant X2
sodium-independent sulfate anion transporter-like, transcript variant X3
sodium-independent sulfate anion transporter-like, transcript variant X1
sodium-independent sulfate anion transporter-like
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
sodium-independent sulfate anion transporter
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC122632927, transcript variant X2
uncharacterized LOC122632927, transcript variant X1
uncharacterized LOC122632920, transcript variant X2
uncharacterized LOC122632920, transcript variant X3
peptidyl-tRNA hydrolase ICT1, mitochondrial
uncharacterized protein LOC122632920 isoform X2
uncharacterized LOC122632920, transcript variant X1
uncharacterized protein LOC122632920 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 97% 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 92% 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: uncharacterized protein LOC122632898
uncharacterized LOC122632922, 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 1 sample with support for all annotated introns
uncharacterized LOC122632922, transcript variant X2
exodeoxyribonuclease, transcript variant X3
exodeoxyribonuclease, transcript variant X2
exodeoxyribonuclease, transcript variant X1
uncharacterized LOC122632919, 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 22 samples with support for all annotated introns
uncharacterized LOC122632919, 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 14 samples with support for all annotated introns
uncharacterized protein LOC122632919 isoform X1
uncharacterized protein LOC122632919 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
uncharacterized protein MAL13P1.304-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58% coverage of the annotated genomic feature by RNAseq alignments
putative uncharacterized protein DDB_G0282133, transcript variant X1
putative uncharacterized protein DDB_G0282133, transcript variant X2
putative uncharacterized protein DDB_G0282133, transcript variant X3
putative uncharacterized protein DDB_G0282133 isoform X1
putative uncharacterized protein DDB_G0282133 isoform X2
CDAN1-interacting nuclease 1, transcript variant X2
CDAN1-interacting nuclease 1, transcript variant X1
uncharacterized LOC122633067, transcript variant X2
uncharacterized LOC122633067, transcript variant X3
uncharacterized LOC122633067, transcript variant X1
uncharacterized protein LOC122633067 isoform X1
uncharacterized LOC122633067, transcript variant X4
uncharacterized LOC122633067, transcript variant X5
uncharacterized protein LOC122633067 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 31 samples with support for all annotated introns
neurochondrin homolog, transcript variant X1
neurochondrin homolog, transcript variant X3
neurochondrin homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
uncharacterized LOC122633061, transcript variant X1
uncharacterized LOC122633061, transcript variant X2
uncharacterized LOC122633061, transcript variant X4
uncharacterized LOC122633061, transcript variant X3
uncharacterized protein LOC122633061 isoform X1
uncharacterized protein LOC122633061 isoform X2
uncharacterized protein LOC122633061 isoform X3
alpha-methylacyl-CoA racemase, transcript variant X1
alpha-methylacyl-CoA racemase, 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 45 samples with support for all annotated introns
alpha-methylacyl-CoA racemase isoform X2
alpha-methylacyl-CoA racemase isoform X1
Golgi pH regulator, transcript variant X3
Golgi pH regulator, transcript variant X4
endoplasmic reticulum-Golgi intermediate compartment protein 2 isoform X3
Golgi pH regulator, transcript variant X2
Golgi pH regulator, transcript variant X1
chondroitin sulfate proteoglycan 4, transcript variant X2
chondroitin sulfate proteoglycan 4, transcript variant X6
chondroitin sulfate proteoglycan 4, transcript variant X1
chondroitin sulfate proteoglycan 4, transcript variant X7
chondroitin sulfate proteoglycan 4, transcript variant X4
chondroitin sulfate proteoglycan 4, transcript variant X5
chondroitin sulfate proteoglycan 4, transcript variant X8
chondroitin sulfate proteoglycan 4, transcript variant X3
chondroitin sulfate proteoglycan 4 isoform X1
chondroitin sulfate proteoglycan 4 isoform X2
sodium/potassium/calcium exchanger Nckx30C, 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 22 samples with support for all annotated introns
sodium/potassium/calcium exchanger Nckx30C, transcript variant X3
sodium/potassium/calcium exchanger Nckx30C, transcript variant X2
sodium/potassium/calcium exchanger Nckx30C, 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 17 samples with support for all annotated introns
sodium/potassium/calcium exchanger Nckx30C, transcript variant X5
sodium/potassium/calcium exchanger Nckx30C, transcript variant X6
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
sodium/potassium/calcium exchanger Nckx30C isoform X1
sodium/potassium/calcium exchanger Nckx30C isoform X3
sodium/potassium/calcium exchanger Nckx30C isoform X2
sodium/potassium/calcium exchanger Nckx30C isoform X4
sodium/potassium/calcium exchanger Nckx30C isoform X5
sodium/potassium/calcium exchanger Nckx30C isoform X6
DNA methyltransferase 1-associated protein 1
uncharacterized LOC122632989, transcript variant X3
uncharacterized LOC122632989, transcript variant X2
uncharacterized LOC122632989, transcript variant X1
uncharacterized protein LOC122632989 isoform X1
uncharacterized protein LOC122632989 isoform X2
cytosolic carboxypeptidase 1-like, transcript variant X8
cytosolic carboxypeptidase 1-like, transcript variant X2
cytosolic carboxypeptidase 1-like, transcript variant X7
cytosolic carboxypeptidase 1-like, transcript variant X9
cytosolic carboxypeptidase 1-like, transcript variant X10
cytosolic carboxypeptidase 1-like, transcript variant X12
cytosolic carboxypeptidase 1-like, transcript variant X13
cytosolic carboxypeptidase 1-like, transcript variant X4
cytosolic carboxypeptidase 1-like, transcript variant X1
cytosolic carboxypeptidase 1-like, transcript variant X3
cytosolic carboxypeptidase 1-like isoform X2
cytosolic carboxypeptidase 1-like isoform X1
cytosolic carboxypeptidase 1-like isoform X7
cytosolic carboxypeptidase 1-like isoform X8
cytosolic carboxypeptidase 1-like isoform X5
cytosolic carboxypeptidase 1-like, transcript variant X5
cytosolic carboxypeptidase 1-like, transcript variant X6
cytosolic carboxypeptidase 1-like isoform X3
cytosolic carboxypeptidase 1-like isoform X4
cytosolic carboxypeptidase 1-like, transcript variant X11
cytosolic carboxypeptidase 1-like isoform 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 29 samples with support for all annotated introns
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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 18 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 2 samples with support for all annotated introns
uncharacterized LOC122633029, transcript variant X1
uncharacterized LOC122633029, transcript variant X12
uncharacterized LOC122633029, transcript variant X19
uncharacterized LOC122633029, transcript variant X4
uncharacterized LOC122633029, transcript variant X17
uncharacterized LOC122633029, transcript variant X8
uncharacterized protein LOC122633029 isoform X1
uncharacterized LOC122633029, transcript variant X2
uncharacterized LOC122633029, transcript variant X3
uncharacterized LOC122633029, transcript variant X18
uncharacterized protein LOC122633029 isoform X2
uncharacterized LOC122633029, transcript variant X9
uncharacterized LOC122633029, transcript variant X10
uncharacterized LOC122633029, transcript variant X13
uncharacterized LOC122633029, transcript variant X7
uncharacterized LOC122633029, transcript variant X6
uncharacterized LOC122633029, transcript variant X5
uncharacterized LOC122633029, transcript variant X15
uncharacterized LOC122633029, transcript variant X11
uncharacterized LOC122633029, transcript variant X14
uncharacterized LOC122633029, transcript variant X16
39S ribosomal protein L22, mitochondrial
nitrilase and fragile histidine triad fusion protein NitFhit, transcript variant X3
nitrilase and fragile histidine triad fusion protein NitFhit, transcript variant X1
nitrilase and fragile histidine triad fusion protein NitFhit isoform X1
nitrilase and fragile histidine triad fusion protein NitFhit, transcript variant X2
nitrilase and fragile histidine triad fusion protein NitFhit isoform X2
TBC1 domain family member whacked, transcript variant X2
TBC1 domain family member whacked, transcript variant X1
TBC1 domain family member whacked, transcript variant X3
uncharacterized LOC122632900, transcript variant X1
uncharacterized LOC122632900, transcript variant X2
low-density lipoprotein receptor-related protein 6, transcript variant X2
low-density lipoprotein receptor-related protein 6, transcript variant X1
low-density lipoprotein receptor-related protein 6
probable tubulin polyglutamylase TTLL1, 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 14 samples with support for all annotated introns
probable tubulin polyglutamylase TTLL1, 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 1 sample with support for all annotated introns
probable tubulin polyglutamylase TTLL1, transcript variant 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 10 samples with support for all annotated introns
probable tubulin polyglutamylase TTLL1 isoform X1
probable tubulin polyglutamylase TTLL1 isoform X2
probable tubulin polyglutamylase TTLL1 isoform X3
probable 39S ribosomal protein L23, mitochondrial
uncharacterized LOC122632847, transcript variant X2
uncharacterized LOC122632847, transcript variant X3
uncharacterized LOC122632847, transcript variant X1
uncharacterized protein LOC122632847 isoform X1
uncharacterized protein LOC122632847 isoform X2
uncharacterized protein LOC122632847 isoform 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 15 samples with support for all annotated introns
4'-phosphopantetheine phosphatase, 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 22 samples with support for all annotated introns
4'-phosphopantetheine phosphatase, 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 39 samples with support for all annotated introns
4'-phosphopantetheine phosphatase isoform X1
4'-phosphopantetheine phosphatase isoform 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 33 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 25 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 18 samples with support for all annotated introns
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 19 samples with support for all annotated introns
ribonucleoside-diphosphate reductase large subunit, transcript variant X1
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 19 samples with support for all annotated introns
ribonucleoside-diphosphate reductase large subunit, 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, including 7 samples with support for all annotated introns
ribonucleoside-diphosphate reductase large subunit, transcript variant 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 22 samples with support for all annotated introns
ribonucleoside-diphosphate reductase large subunit
zinc finger protein 436-like, transcript variant X5
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 26 samples with support for all annotated introns
zinc finger protein 436-like, transcript variant X6
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 23 samples with support for all annotated introns
zinc finger protein 436-like, 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 40 samples with support for all annotated introns
zinc finger protein 436-like, transcript variant X4
zinc finger protein 436-like, 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 12 samples with support for all annotated introns
zinc finger protein 436-like, transcript variant X2
zinc finger protein 436-like, transcript variant 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 22 samples with support for all annotated introns
AN1-type zinc finger protein 2A-like, transcript variant X2
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 20 samples with support for all annotated introns
AN1-type zinc finger protein 2A-like, transcript variant 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, including 39 samples with support for all annotated introns
RNA transcription, translation and transport factor protein, transcript variant X2
RNA transcription, translation and transport factor protein, transcript variant X1
RNA transcription, translation and transport factor protein isoform X2
RNA transcription, translation and transport factor protein isoform X1
ran-binding protein 9, transcript variant X2
ran-binding protein 9, transcript variant X4
ran-binding protein 9, transcript variant X5
ran-binding protein 9, transcript variant X1
ran-binding protein 9, transcript variant X3
ran-binding protein 9, transcript variant X6
ran-binding protein 9, transcript variant X7
protein bric-a-brac 2-like, 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
protein bric-a-brac 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 24 samples with support for all annotated introns
protein bric-a-brac 2-like, 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 32 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X6
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 8 samples with support for all annotated introns
protein bric-a-brac 2-like, transcript variant X5
protein bric-a-brac 2-like, transcript variant X3
protein bric-a-brac 2-like, transcript variant X7
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 5 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 34-like isoform X1
zinc finger and BTB domain-containing protein 34-like 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 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 15 samples with support for all annotated introns
protein retinal degeneration B, transcript variant X6
protein retinal degeneration B, transcript variant X5
protein retinal degeneration B, transcript variant X4
protein retinal degeneration B, transcript variant X1
protein retinal degeneration B, transcript variant X3
protein retinal degeneration B, transcript variant X2
protein retinal degeneration B isoform X6
protein retinal degeneration B isoform X5
protein retinal degeneration B isoform X4
protein retinal degeneration B isoform X1
protein retinal degeneration B isoform X3
protein retinal degeneration B isoform X2
protein retinal degeneration B, transcript variant X10
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 15 samples with support for all annotated introns
protein retinal degeneration B, transcript variant X8
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 21 samples with support for all annotated introns
protein retinal degeneration B, transcript variant X11
protein retinal degeneration B, transcript variant X7
protein retinal degeneration B isoform X8
protein retinal degeneration B, transcript variant X9
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 12 samples with support for all annotated introns
protein retinal degeneration B isoform X7
uncharacterized LOC122633036, transcript variant X6
uncharacterized LOC122633036, transcript variant X5
uncharacterized LOC122633036, transcript variant X7
uncharacterized LOC122633036, transcript variant X4
uncharacterized LOC122633036, transcript variant X2
uncharacterized LOC122633036, transcript variant X3
uncharacterized LOC122633036, transcript variant X1
uncharacterized protein LOC122633036 isoform X1
uncharacterized protein LOC122633036 isoform X2
facilitated trehalose transporter Tret1-like
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 5 samples with support for all annotated introns
cytochrome P450 4C1-like, transcript variant X1
cytochrome P450 4C1-like, transcript variant X2
facilitated trehalose transporter Tret1, transcript variant X2
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 46 samples with support for all annotated introns
facilitated trehalose transporter Tret1, 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 43 samples with support for all annotated introns
facilitated trehalose transporter Tret1 isoform X1
facilitated trehalose transporter Tret1 isoform X2
octopamine receptor beta-3R-like, transcript variant X6
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 15 samples with support for all annotated introns
octopamine receptor beta-3R-like, transcript variant X5
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
octopamine receptor beta-3R-like, transcript variant X4
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 7 samples with support for all annotated introns
octopamine receptor beta-3R-like, transcript variant X3
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 18 samples with support for all annotated introns
octopamine receptor beta-3R-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 4 samples with support for all annotated introns
octopamine receptor beta-3R-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 36 samples with support for all annotated introns
octopamine receptor beta-3R-like isoform X3
octopamine receptor beta-3R-like isoform X2
octopamine receptor beta-3R-like isoform X1
cell growth regulator with RING finger domain protein 1-like
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 44 samples with support for all annotated introns
uncharacterized LOC122633131, transcript variant X2
uncharacterized LOC122633131, transcript variant X1
uncharacterized LOC122633131, transcript variant X3
GATA-binding factor A-like, transcript variant X2
GATA-binding factor A-like, transcript variant X1
GATA-binding factor A-like, transcript variant X3
GATA-binding factor A-like, transcript variant X4
nuclear receptor subfamily 2 group E member 1, transcript variant X3
nuclear receptor subfamily 2 group E member 1, transcript variant X1
nuclear receptor subfamily 2 group E member 1, transcript variant X2
nuclear receptor subfamily 2 group E member 1 isoform X1
nuclear receptor subfamily 2 group E member 1 isoform X2
nuclear receptor subfamily 2 group E member 1 isoform X3
rho GTPase-activating protein conundrum, transcript variant X2
rho GTPase-activating protein conundrum, transcript variant X1
rho GTPase-activating protein conundrum, transcript variant X3
serine/threonine-protein phosphatase 6 regulatory subunit 3, transcript variant X7
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 37 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory subunit 3, transcript variant X4
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 39 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory subunit 3, 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 37 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory subunit 3, transcript variant X2
serine/threonine-protein phosphatase 6 regulatory subunit 3, transcript variant X3
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 17 samples with support for all annotated introns
serine/threonine-protein phosphatase 6 regulatory subunit 3, transcript variant X1
serine/threonine-protein phosphatase 6 regulatory subunit 3, transcript variant X5
serine/threonine-protein phosphatase 6 regulatory subunit 3 isoform X3
serine/threonine-protein phosphatase 6 regulatory subunit 3 isoform X5
serine/threonine-protein phosphatase 6 regulatory subunit 3 isoform X2
serine/threonine-protein phosphatase 6 regulatory subunit 3 isoform X4
serine/threonine-protein phosphatase 6 regulatory subunit 3 isoform X1
ras-related protein rab7, transcript variant X2
ras-related protein rab7, transcript variant X1
DNA topoisomerase 2, transcript variant X2
DNA topoisomerase 2, transcript variant X1
DNA topoisomerase 2, transcript variant X3
serine/threonine-protein kinase tousled-like 2, transcript variant X3
serine/threonine-protein kinase tousled-like 2, transcript variant X6
serine/threonine-protein kinase tousled-like 2, transcript variant X5
serine/threonine-protein kinase tousled-like 2, transcript variant X4
serine/threonine-protein kinase tousled-like 2, transcript variant X7
serine/threonine-protein kinase tousled-like 2, transcript variant X15
serine/threonine-protein kinase tousled-like 2, transcript variant X14
serine/threonine-protein kinase tousled-like 2, transcript variant X11
serine/threonine-protein kinase tousled-like 2, transcript variant X2
serine/threonine-protein kinase tousled-like 2, transcript variant X1
serine/threonine-protein kinase tousled-like 2, transcript variant X16
serine/threonine-protein kinase tousled-like 2, transcript variant X10
serine/threonine-protein kinase tousled-like 2, transcript variant X9
serine/threonine-protein kinase tousled-like 2, transcript variant X8
serine/threonine-protein kinase tousled-like 2, transcript variant X17
serine/threonine-protein kinase tousled-like 2, transcript variant X12
serine/threonine-protein kinase tousled-like 2, transcript variant X13
serine/threonine-protein kinase tousled-like 2 isoform X3
serine/threonine-protein kinase tousled-like 2 isoform X4
serine/threonine-protein kinase tousled-like 2 isoform X8
serine/threonine-protein kinase tousled-like 2 isoform X7
serine/threonine-protein kinase tousled-like 2 isoform X6
serine/threonine-protein kinase tousled-like 2 isoform X5
serine/threonine-protein kinase tousled-like 2 isoform X2
serine/threonine-protein kinase tousled-like 2 isoform X1
serine/threonine-protein kinase tousled-like 2 isoform X9
serine/threonine-protein kinase tousled-like 2 isoform X10
late secretory pathway protein AVL9 homolog
VPS35 endosomal protein-sorting factor-like
4-aminobutyrate aminotransferase, mitochondrial
uncharacterized LOC122633166, transcript variant X1
uncharacterized LOC122633166, transcript variant X2
uncharacterized LOC122633166, 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 5 samples with support for all annotated introns
uncharacterized LOC122633166, transcript variant X3
uncharacterized LOC122633165, transcript variant X4
uncharacterized LOC122633165, transcript variant X3
uncharacterized LOC122633165, transcript variant X1
uncharacterized LOC122633165, transcript variant X2
uncharacterized protein LOC122633165 isoform X3
uncharacterized protein LOC122633165 isoform X2
uncharacterized protein LOC122633165 isoform X1
MICAL-like protein 1, transcript variant X2
MICAL-like protein 1, transcript variant X3
MICAL-like protein 1, transcript variant X1
MICAL-like protein 1, transcript variant X5
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 40 samples with support for all annotated introns
MICAL-like protein 1, transcript variant X4
protein-lysine N-methyltransferase EEF2KMT
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
WASH complex subunit 4, transcript variant X1
WASH complex subunit 4, transcript variant X2
G patch domain and ankyrin repeat-containing protein 1 homolog
calcium and integrin-binding family member 2-like, transcript variant X2
calcium and integrin-binding family member 2-like, transcript variant X1
calcium and integrin-binding family member 2-like isoform X1
calcium and integrin-binding family member 2-like isoform X2
28S ribosomal protein S36, mitochondrial, transcript variant X2
28S ribosomal protein S36, mitochondrial, transcript variant X1
28S ribosomal protein S36, mitochondrial isoform X1
28S ribosomal protein S36, mitochondrial isoform X2
high mobility group nucleosome-binding domain-containing protein 5-like, transcript variant X3
high mobility group nucleosome-binding domain-containing protein 5-like, transcript variant X2
high mobility group nucleosome-binding domain-containing protein 5-like, transcript variant X1
high mobility group nucleosome-binding domain-containing protein 5-like, transcript variant X4
probable inactive protein kinase DDB_G0270444 isoform X1
probable inactive protein kinase DDB_G0270444 isoform X3
high mobility group nucleosome-binding domain-containing protein 5-like isoform X4
mitochondrial inner membrane protease subunit 2, 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 36 samples with support for all annotated introns
mitochondrial inner membrane protease subunit 2, 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 34 samples with support for all annotated introns
mitochondrial inner membrane protease subunit 2
sodium-coupled monocarboxylate transporter 1-like, transcript variant X1
sodium-coupled monocarboxylate transporter 1-like, transcript variant X4
sodium-coupled monocarboxylate transporter 1-like, transcript variant X2
sodium-coupled monocarboxylate transporter 1-like, transcript variant X3
sodium-coupled monocarboxylate transporter 1-like
homeobox protein OTX2-B-like, transcript variant X2
homeobox protein OTX2-B-like, transcript variant X1
homeobox protein OTX2-B-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 26 samples with support for all annotated introns
E3 ubiquitin-protein ligase Nedd-4, transcript variant X3
E3 ubiquitin-protein ligase Nedd-4, transcript variant X2
E3 ubiquitin-protein ligase Nedd-4, transcript variant X1
E3 ubiquitin-protein ligase Nedd-4, transcript variant X5
E3 ubiquitin-protein ligase Nedd-4, transcript variant X4
E3 ubiquitin-protein ligase NEDD4 isoform X3
E3 ubiquitin-protein ligase Nedd-4 isoform X1
E3 ubiquitin-protein ligase Nedd-4 isoform X2
iron-sulfur cluster assembly scaffold protein IscU, transcript variant X1
iron-sulfur cluster assembly scaffold protein IscU isoform X1
iron-sulfur cluster assembly scaffold protein IscU, transcript variant X2
iron-sulfur cluster assembly scaffold protein IscU isoform X2
NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial
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 23 samples with support for all annotated introns
uncharacterized LOC122632793, transcript variant X4
uncharacterized LOC122632793, transcript variant X2
uncharacterized LOC122632793, transcript variant X3
uncharacterized LOC122632793, transcript variant X1
uncharacterized protein LOC122632793 isoform X1
uncharacterized protein LOC122632793 isoform X2
uncharacterized LOC122632793, transcript variant X5
uncharacterized protein LOC122632793 isoform X3
uncharacterized LOC122632793, transcript variant X6
uncharacterized protein LOC122632793 isoform 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 19 samples with support for all annotated introns
U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit-related protein 1, transcript variant X3
U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit-related protein 1, transcript variant X2
U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit-related protein 1, transcript variant X1
U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit-related protein 1 isoform X1
U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit-related protein 1 isoform X3
U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit-related protein 1 isoform X2
uncharacterized LOC122632963, transcript variant X2
uncharacterized LOC122632963, transcript variant X1
uncharacterized LOC122632963, transcript variant X3
uncharacterized protein LOC122632963 isoform X1
uncharacterized protein LOC122632963 isoform X2
probable G-protein coupled receptor B0563.6, transcript variant X1
probable G-protein coupled receptor B0563.6, transcript variant X2
probable G-protein coupled receptor B0563.6, transcript variant X3
probable G-protein coupled receptor B0563.6
uncharacterized LOC122632763, transcript variant X2
uncharacterized LOC122632763, transcript variant X1
uncharacterized protein LOC122632763 isoform X1
uncharacterized protein LOC122632763 isoform X2
ras guanine nucleotide exchange factor P-like, transcript variant X1
ras guanine nucleotide exchange factor P-like, transcript variant X2
ras guanine nucleotide exchange factor P-like isoform X1
ras guanine nucleotide exchange factor P-like isoform X2
zinc finger protein 329-like, transcript variant X1
zinc finger protein 329-like, transcript variant X2
zinc finger protein 329-like, transcript variant X3
thioredoxin domain-containing protein 15
glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1
mediator of RNA polymerase II transcription subunit 13, transcript variant X4
mediator of RNA polymerase II transcription subunit 13, transcript variant X3
mediator of RNA polymerase II transcription subunit 13, transcript variant X2
mediator of RNA polymerase II transcription subunit 13, transcript variant X1
mediator of RNA polymerase II transcription subunit 13 isoform X4
mediator of RNA polymerase II transcription subunit 13 isoform X3
mediator of RNA polymerase II transcription subunit 13 isoform X2
mediator of RNA polymerase II transcription subunit 13 isoform X1
39S ribosomal protein L50, mitochondrial
uncharacterized LOC122632867, transcript variant X1
uncharacterized LOC122632867, transcript variant X2
uncharacterized protein LOC122632867 isoform X1
uncharacterized protein LOC122632867 isoform X2
G protein-coupled receptor kinase 1, transcript variant X1
G protein-coupled receptor kinase 1, transcript variant X2
G protein-coupled receptor kinase 1, transcript variant X3
G protein-coupled receptor kinase 1 isoform X1
G protein-coupled receptor kinase 1 isoform X2
G protein-coupled receptor kinase 1 isoform X3
uncharacterized LOC122632863, transcript variant X3
uncharacterized LOC122632863, transcript variant X2
uncharacterized LOC122632863, transcript variant X1
uncharacterized protein LOC122632863 isoform X3
uncharacterized protein LOC122632863 isoform X2
uncharacterized protein LOC122632863 isoform X1
WD repeat and FYVE domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 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: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
suppressor of hairless protein, transcript variant X4
suppressor of hairless protein, transcript variant X3
suppressor of hairless protein, transcript variant X2
suppressor of hairless protein, transcript variant X1
glutathione hydrolase 1 proenzyme-like, transcript variant X1
glutathione hydrolase 1 proenzyme-like, transcript variant X2
glutathione hydrolase 1 proenzyme-like, transcript variant X3
glutathione hydrolase 1 proenzyme-like isoform X1
glutathione hydrolase 1 proenzyme-like isoform X2
glutathione hydrolase 1 proenzyme-like, transcript variant X4
glutathione hydrolase 1 proenzyme-like isoform X3
venom serine protease-like, transcript variant X2
venom serine protease-like, transcript variant X1
uncharacterized LOC122632787, transcript variant X2
uncharacterized LOC122632787, transcript variant X1
uncharacterized LOC122632780, transcript variant X1
uncharacterized LOC122632780, transcript variant X2