Vespa velutina chromosome 23, iVesVel2.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Apocrita; Aculeata; Vespoidea; Vespidae; Vespinae; Vespa.
REFSEQ INFORMATION: The reference sequence is identical to\nOU525145.1.\nAssembly name: iVesVel2.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/08/14. The original whole-genome shotgun project has the\naccession CAJVVP000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Vespa velutina Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
protein crooked neck, 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 7 samples with support for all annotated introns
protein crooked neck, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
L-lactate dehydrogenase B chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
L-lactate dehydrogenase B chain-like, 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
L-lactate dehydrogenase B chain-like, transcript variant X3
L-lactate dehydrogenase B chain-like isoform X1
L-lactate dehydrogenase B-B chain-like isoform X2
bestrophin homolog 15, transcript variant X1
bestrophin homolog 15, transcript variant X2
uncharacterized protein LOC124956630 isoform X2
uncharacterized LOC124956726, transcript variant X1
uncharacterized protein LOC124956726 isoform X1
uncharacterized LOC124956726, transcript variant X4
uncharacterized LOC124956726, transcript variant X3
uncharacterized LOC124956726, transcript variant X2
uncharacterized protein LOC124956726 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 5 samples with support for all annotated introns
uncharacterized protein LOC124956726 isoform X3
Krueppel-like factor 6, transcript variant X3
Krueppel-like factor 6, transcript variant X2
Krueppel-like factor 6, transcript variant X1
Krueppel-like factor 6, transcript variant X4
Krueppel-like factor 6, transcript variant X5
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 2 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 7 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
protein BEAN1-like, transcript variant X2
protein BEAN1-like, transcript variant X3
protein BEAN1-like, transcript variant X1
E3 SUMO-protein ligase CBX4-like isoform X2
polycomb group protein Pc-like isoform X1
E3 SUMO-protein ligase CBX4-like isoform X3
protein BEAN1-like, transcript variant X4
uncharacterized LOC124956745, transcript variant X1
uncharacterized LOC124956745, transcript variant X3
uncharacterized LOC124956745, transcript variant X2
farnesol dehydrogenase-like, transcript variant X2
farnesol dehydrogenase-like, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC124956711, transcript variant X1
uncharacterized LOC124956711, transcript variant X2
uncharacterized protein LOC124956711 isoform X1
uncharacterized protein LOC124956711 isoform X2
uncharacterized protein DDB_G0287625-like, 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 5 samples with support for all annotated introns
ras guanine nucleotide exchange factor P-like isoform X2
uncharacterized protein DDB_G0287625-like, transcript variant X1
uncharacterized protein DDB_G0287625-like isoform 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 2 samples with support for all annotated introns
uncharacterized LOC124956714, transcript variant X2
uncharacterized LOC124956714, transcript variant X1
uncharacterized LOC124956714, transcript variant X3
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
coiled-coil domain-containing protein 6, transcript variant X1
coiled-coil domain-containing protein 6, transcript variant X2
coiled-coil domain-containing protein 6 isoform X2
coiled-coil domain-containing protein 6 isoform X1
calcium uptake protein 1 homolog, mitochondrial, 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 7 samples with support for all annotated introns
calcium uptake protein 1 homolog, mitochondrial, transcript variant X5
calcium uptake protein 1 homolog, mitochondrial, transcript variant X4
calcium uptake protein 1 homolog, mitochondrial, transcript variant X3
calcium uptake protein 1 homolog, mitochondrial, transcript variant X1
calcium uptake protein 1 homolog, mitochondrial isoform X3
calcium uptake protein 1 homolog, mitochondrial isoform X2
calcium uptake protein 1 homolog, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); 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: 57 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
recQ-mediated genome instability protein 1-like, transcript variant X2
recQ-mediated genome instability protein 1-like, transcript variant X1
recQ-mediated genome instability protein 1-like isoform X2
recQ-mediated genome instability protein 1-like isoform X1
uncharacterized LOC124956753, transcript variant X3
uncharacterized LOC124956753, transcript variant X1
uncharacterized LOC124956753, transcript variant X2
uncharacterized protein LOC124956753 isoform X1
uncharacterized protein LOC124956753 isoform X2
uncharacterized protein LOC124956753 isoform X3
chromatin modification-related protein MEAF6
cuticle protein 19-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cuticle protein 19-like, transcript variant X3
cuticle protein 19-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
28S ribosomal protein S15, mitochondrial
uncharacterized LOC124956754, transcript variant X2
uncharacterized LOC124956754, transcript variant X4
uncharacterized LOC124956754, transcript variant X3
uncharacterized LOC124956754, transcript variant X5
uncharacterized LOC124956754, transcript variant X1
uncharacterized LOC124956754, transcript variant X7
uncharacterized protein LOC124956754 isoform X1
uncharacterized protein LOC124956754 isoform X3
uncharacterized LOC124956754, transcript variant X6
uncharacterized protein LOC124956754 isoform X2
probable ribonuclease ZC3H12C, 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 4 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 45
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable ribonuclease ZC3H12C, transcript variant X3
probable ribonuclease ZC3H12C, transcript variant X1
probable ribonuclease ZC3H12C, transcript variant X6
probable ribonuclease ZC3H12C, transcript variant X4
probable ribonuclease ZC3H12C, transcript variant X5
probable ribonuclease ZC3H12C isoform X3
probable ribonuclease ZC3H12C isoform X4
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124956789, transcript variant X2
odorant receptor 30a-like, 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
odorant receptor 30a-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 1 sample with support for all annotated introns
uncharacterized LOC124956789, 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cuticle protein 7-like, transcript variant X3
cuticle protein 7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cuticle protein 7-like, transcript variant X1
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 3 samples with support for all annotated introns
uncharacterized protein LOC124956786 isoform X1
cuticle protein 7-like, transcript variant X4
cuticle protein 7-like, transcript variant X5
uncharacterized protein LOC124956786 isoform X3
uncharacterized LOC124956788, transcript variant X2
uncharacterized LOC124956788, transcript variant X1
cell adhesion molecule 2-like, transcript variant X7
cell adhesion molecule 2-like, transcript variant X4
cell adhesion molecule 2-like, transcript variant X5
cell adhesion molecule 2-like, transcript variant X2
cell adhesion molecule 2-like, transcript variant X3
cell adhesion molecule 2-like, transcript variant X6
cell adhesion molecule 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 2 samples with support for all annotated introns
adult-specific cuticular protein ACP-22-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, 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 5 samples with support for all annotated introns
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X2
D-beta-hydroxybutyrate dehydrogenase, mitochondrial, transcript variant X1
D-beta-hydroxybutyrate dehydrogenase, mitochondrial
tRNA N(3)-methylcytidine methyltransferase METTL6, 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 3 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6, transcript variant X1
tRNA N(3)-methylcytidine methyltransferase METTL6
small nucleolar RNA snR60/Z15/Z230/Z193/J17
COORDINATES: nucleotide motif:Rfam:12.0:RF00309
uncharacterized LOC124956679, 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 3 samples with support for all annotated introns
uncharacterized LOC124956679, 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 2 samples with support for all annotated introns
uncharacterized protein LOC124956679 isoform X1
uncharacterized protein LOC124956679 isoform X2
keratin, type I cytoskeletal 9-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
keratin, type I cytoskeletal 9-like, transcript variant X2
keratin, type I cytoskeletal 9-like isoform X1
rac guanine nucleotide exchange factor JJ-like
putative uncharacterized protein DDB_G0282129, 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 3 samples with support for all annotated introns
putative uncharacterized protein DDB_G0282129 isoform X2
putative uncharacterized protein DDB_G0282129, transcript variant X3
putative uncharacterized protein DDB_G0282129, transcript variant X1
putative uncharacterized protein DDB_G0282129 isoform X1
putative uncharacterized protein DDB_G0282129 isoform X3
nuclear pore complex protein DDB_G0274915-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear pore complex protein DDB_G0274915-like, transcript variant X2
nuclear pore complex protein DDB_G0274915-like isoform X1
nuclear pore complex protein DDB_G0274915-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 3% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 96% coverage of the annotated genomic feature by RNAseq alignments
keratin, type II cytoskeletal 1-like, 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 1 sample with support for all annotated introns
keratin, type II cytoskeletal 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 2 samples with support for all annotated introns
keratin, type II cytoskeletal 1-like isoform X2
uncharacterized protein LOC124956671 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X5
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X4
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like, transcript variant X3
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X3
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
dopamine D2-like receptor, transcript variant X5
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 3 samples with support for all annotated introns
dopamine D2-like receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dopamine D2-like receptor, transcript variant X6
dopamine D2-like receptor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dopamine D2-like receptor, 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 2 samples with support for all annotated introns
dopamine D2-like receptor, transcript variant X3
igLON family member 5-like, transcript variant X1
igLON family member 5-like, transcript variant X2
igLON family member 5-like, transcript variant X3
inactive tyrosine-protein kinase 7-like, transcript variant X5
inactive tyrosine-protein kinase 7-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
inactive tyrosine-protein kinase 7-like, transcript variant X1
inactive tyrosine-protein kinase 7-like, transcript variant X2
inactive tyrosine-protein kinase 7-like, transcript variant X4
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
immunoglobulin superfamily member 10-like isoform X1
inactive tyrosine-protein kinase 7-like isoform X2
uncharacterized LOC124956667, transcript variant X3
uncharacterized LOC124956667, transcript variant X2
uncharacterized LOC124956667, transcript variant X1
mitochondrial dicarboxylate carrier, transcript variant X1
mitochondrial dicarboxylate carrier, transcript variant X2
mitochondrial dicarboxylate carrier, transcript variant X3
mitochondrial dicarboxylate carrier isoform X1
mitochondrial dicarboxylate carrier isoform X2
spliceosome-associated protein CWC27 homolog, transcript variant X1
spliceosome-associated protein CWC27 homolog isoform X1
spliceosome-associated protein CWC27 homolog, transcript variant X2
spliceosome-associated protein CWC27 homolog isoform X2
dynein axonemal assembly factor 11, transcript variant X6
dynein axonemal assembly factor 11, transcript variant X5
dynein axonemal assembly factor 11, transcript variant X3
dynein axonemal assembly factor 11, transcript variant X1
dynein axonemal assembly factor 11, transcript variant X2
dynein axonemal assembly factor 11, transcript variant X4
dynein axonemal assembly factor 11 isoform X3
dynein axonemal assembly factor 11 isoform X1
dynein axonemal assembly factor 11 isoform X2
BTB/POZ domain-containing protein KCTD3, transcript variant X3
BTB/POZ domain-containing protein KCTD3, transcript variant X1
BTB/POZ domain-containing protein KCTD3, transcript variant X2
BTB/POZ domain-containing protein KCTD3 isoform X1
BTB/POZ domain-containing protein KCTD3 isoform X2
BTB/POZ domain-containing protein KCTD3 isoform X3
CAAX prenyl protease 2, transcript variant X1
CAAX prenyl protease 2, transcript variant X2
CAAX prenyl protease 2, transcript variant X3
F-box only protein 11, transcript variant X4
F-box only protein 11, transcript variant X1
F-box only protein 11, transcript variant X2
F-box only protein 11, transcript variant X3
mediator of RNA polymerase II transcription subunit 6
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 7 samples with support for all annotated introns
pyridoxal phosphate phosphatase PHOSPHO2-like, transcript variant X2
pyridoxal phosphate phosphatase PHOSPHO2-like, transcript variant X3
pyridoxal phosphate phosphatase PHOSPHO2-like, transcript variant X1
pyridoxal phosphate phosphatase PHOSPHO2-like
putative ATP synthase subunit f, mitochondrial
host cell factor 1, transcript variant X1
host cell factor 1, transcript variant X2
host cell factor 1, transcript variant X3
host cell factor 1, transcript variant X4
uncharacterized LOC124956803, transcript variant X2
uncharacterized LOC124956803, transcript variant X3
uncharacterized LOC124956803, transcript variant X1
uncharacterized LOC124956803, transcript variant X7
uncharacterized LOC124956803, transcript variant X4
uncharacterized LOC124956803, transcript variant X6
uncharacterized LOC124956803, 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 7 samples with support for all annotated introns
uncharacterized protein LOC124956803 isoform X1
uncharacterized protein LOC124956803 isoform X5
uncharacterized protein LOC124956803 isoform X4
uncharacterized protein LOC124956803 isoform X3
uncharacterized protein LOC124956803 isoform X2
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9
plasma membrane calcium-transporting ATPase 3, transcript variant X1
plasma membrane calcium-transporting ATPase 3, 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
plasma membrane calcium-transporting ATPase 3, 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 1 sample with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X7
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
plasma membrane calcium-transporting ATPase 3, 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 3 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X4
plasma membrane calcium-transporting ATPase 3, transcript variant X3
plasma membrane calcium-transporting ATPase 3, transcript variant X9
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
plasma membrane calcium-transporting ATPase 3, transcript variant X13
plasma membrane calcium-transporting ATPase 3, transcript variant X6
plasma membrane calcium-transporting ATPase 3, 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 7 samples with support for all annotated introns
plasma membrane calcium-transporting ATPase 3, transcript variant X12
plasma membrane calcium-transporting ATPase 3, transcript variant X11
plasma membrane calcium-transporting ATPase 3 isoform X8
plasma membrane calcium-transporting ATPase 2 isoform X4
plasma membrane calcium-transporting ATPase 3 isoform X6
plasma membrane calcium-transporting ATPase 2 isoform X1
plasma membrane calcium-transporting ATPase 2 isoform X3
plasma membrane calcium-transporting ATPase 2 isoform X2
plasma membrane calcium-transporting ATPase 3 isoform X5
plasma membrane calcium-transporting ATPase 3 isoform X7
plasma membrane calcium-transporting ATPase 3 isoform X10
plasma membrane calcium-transporting ATPase 3 isoform X9
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X1
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X4
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X2
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X3
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X6
KN motif and ankyrin repeat domain-containing protein 1, transcript variant X5
KN motif and ankyrin repeat domain-containing protein 1 isoform X1
extracellular matrix-binding protein ebh isoform X3
KN motif and ankyrin repeat domain-containing protein 1 isoform X2
ataxin-7-like protein 1, transcript variant X1
ataxin-7-like protein 1, transcript variant X2
uncharacterized LOC124956687, transcript variant X2
uncharacterized LOC124956687, transcript variant X1
uncharacterized LOC124956687, transcript variant X3
uncharacterized protein LOC124956687 isoform X2
uncharacterized protein LOC124956687 isoform X1
uncharacterized LOC124956687, transcript variant X4
uncharacterized protein LOC124956687 isoform X3
uncharacterized LOC124956689, transcript variant X2
uncharacterized LOC124956689, transcript variant X3
uncharacterized LOC124956689, 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 7 samples with support for all annotated introns
lysine-specific demethylase lid, transcript variant X2
lysine-specific demethylase lid isoform X2
lysine-specific demethylase lid, transcript variant X5
lysine-specific demethylase lid, transcript variant X3
lysine-specific demethylase lid, 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 6 samples with support for all annotated introns
lysine-specific demethylase lid, transcript variant X4
lysine-specific demethylase lid, transcript variant X1
lysine-specific demethylase lid, transcript variant X8
lysine-specific demethylase lid, transcript variant X9
lysine-specific demethylase lid isoform X6
lysine-specific demethylase lid isoform X4
lysine-specific demethylase lid isoform X3
lysine-specific demethylase lid isoform X5
lysine-specific demethylase lid isoform X1
lysine-specific demethylase lid isoform X8
lysine-specific demethylase lid isoform X9
lysine-specific demethylase lid, transcript variant X7
lysine-specific demethylase lid isoform X7
epidermal growth factor receptor kinase substrate 8-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 6 samples with support for all annotated introns
epidermal growth factor receptor kinase substrate 8-like, transcript variant X7
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 5 samples with support for all annotated introns
epidermal growth factor receptor kinase substrate 8-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
epidermal growth factor receptor kinase substrate 8-like, transcript variant X4
epidermal growth factor receptor kinase substrate 8-like, transcript variant X2
epidermal growth factor receptor kinase substrate 8-like, transcript variant X6
epidermal growth factor receptor kinase substrate 8-like, transcript variant X5
epidermal growth factor receptor kinase substrate 8-like isoform X1
epidermal growth factor receptor kinase substrate 8-like protein 2 isoform X2
dihydropyrimidinase, transcript variant X2
dihydropyrimidinase, transcript variant X1
dihydropyrimidinase, transcript variant X3
dihydropyrimidinase, transcript variant X4
ribonuclease H2 subunit C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ribonuclease H2 subunit C, transcript variant X2
serine/threonine-protein kinase Genghis Khan, transcript variant X4
serine/threonine-protein kinase Genghis Khan, transcript variant X3
serine/threonine-protein kinase Genghis Khan, transcript variant X2
serine/threonine-protein kinase Genghis Khan, transcript variant X1
serine/threonine-protein kinase MRCK beta isoform X3
serine/threonine-protein kinase Genghis Khan isoform X1
serine/threonine-protein kinase Genghis Khan isoform X2
deubiquitinase DESI2, transcript variant X2
deubiquitinase DESI2, 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 4 samples with support for all annotated introns
protein MTO1 homolog, mitochondrial, 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 7 samples with support for all annotated introns
protein MTO1 homolog, mitochondrial, 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 5 samples with support for all annotated introns
protein MTO1 homolog, mitochondrial, 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 4 samples with support for all annotated introns
protein MTO1 homolog, mitochondrial, transcript variant X4
protein MTO1 homolog, mitochondrial, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
protein MTO1 homolog, mitochondrial isoform X1
protein MTO1 homolog, mitochondrial isoform X2
protein MTO1 homolog, mitochondrial isoform X3
protein MTO1 homolog, mitochondrial, transcript variant X6
protein MTO1 homolog, mitochondrial, transcript variant X7
protein MTO1 homolog, mitochondrial, transcript variant X8
protein MTO1 homolog, mitochondrial, transcript variant X9
protein MTO1 homolog, mitochondrial isoform X4
protein MTO1 homolog, mitochondrial isoform X5
protein MTO1 homolog, mitochondrial isoform X6
protein MTO1 homolog, mitochondrial isoform X7
probable G-protein coupled receptor Mth-like 1
ATP-dependent DNA/RNA helicase DHX36, transcript variant X2
ATP-dependent DNA/RNA helicase DHX36, transcript variant X1
ATP-dependent DNA/RNA helicase DHX36, transcript variant X3
ATP-dependent DNA/RNA helicase DHX36 isoform X2
ATP-dependent DNA/RNA helicase DHX36 isoform X1
ATP-dependent DNA/RNA helicase DHX36 isoform X3
uracil phosphoribosyltransferase homolog, transcript variant X3
uracil phosphoribosyltransferase homolog, transcript variant X1
uracil phosphoribosyltransferase homolog, transcript variant X2
uracil phosphoribosyltransferase homolog isoform X1
uracil phosphoribosyltransferase homolog isoform X3
uracil phosphoribosyltransferase homolog isoform X2
SH3 domain-binding glutamic acid-rich protein homolog, transcript variant X4
SH3 domain-binding glutamic acid-rich protein homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SH3 domain-binding glutamic acid-rich protein homolog, transcript variant X1
SH3 domain-binding glutamic acid-rich protein homolog, transcript variant X2
SH3 domain-binding glutamic acid-rich protein homolog
polypeptide N-acetylgalactosaminyltransferase 5, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 5, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 5 isoform X2
polypeptide N-acetylgalactosaminyltransferase 5 isoform X1
cytochrome b5 reductase 4, transcript variant X4
cytochrome b5 reductase 4, transcript variant X1
cytochrome b5 reductase 4, transcript variant X3
cytochrome b5 reductase 4, transcript variant X5
cytochrome b5 reductase 4, transcript variant X2
cytochrome b5 reductase 4, transcript variant X9
cytochrome b5 reductase 4, transcript variant X8
cytochrome b5 reductase 4, transcript variant X7
cytochrome b5 reductase 4, transcript variant X6
fatty-acid amide hydrolase 2, transcript variant X5
fatty-acid amide hydrolase 2, transcript variant X9
fatty-acid amide hydrolase 2, transcript variant X10
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 6 samples with support for all annotated introns
fatty-acid amide hydrolase 2, transcript variant X1
fatty-acid amide hydrolase 2, transcript variant X2
fatty-acid amide hydrolase 2, transcript variant X3
fatty-acid amide hydrolase 2, transcript variant X6
fatty-acid amide hydrolase 2, transcript variant X4
fatty-acid amide hydrolase 2, transcript variant X8
fatty-acid amide hydrolase 2, transcript variant X7
androgen-induced gene 1 protein-like, transcript variant X13
androgen-induced gene 1 protein-like, transcript variant X12
androgen-induced gene 1 protein-like, transcript variant X5
androgen-induced gene 1 protein-like, transcript variant X18
androgen-induced gene 1 protein-like, transcript variant X14
androgen-induced gene 1 protein-like, transcript variant X1
androgen-dependent TFPI-regulating protein-like isoform X1
androgen-induced gene 1 protein-like, transcript variant X16
androgen-induced gene 1 protein-like, transcript variant X9
androgen-induced gene 1 protein-like, transcript variant X15
androgen-induced gene 1 protein-like, transcript variant X8
androgen-induced gene 1 protein-like isoform X3
protein smoothened, transcript variant X5
protein smoothened, transcript variant X6
protein smoothened, transcript variant X4
protein smoothened, transcript variant X2
protein smoothened, transcript variant X3
protein smoothened, transcript variant X1
protein smoothened, transcript variant X8
protein smoothened, transcript variant X7
androgen-induced gene 1 protein-like, transcript variant X2
androgen-induced gene 1 protein-like, transcript variant X4
androgen-induced gene 1 protein-like, transcript variant X17
androgen-induced gene 1 protein-like, transcript variant X6
androgen-induced gene 1 protein-like, transcript variant X7
androgen-induced gene 1 protein-like, transcript variant X10
androgen-induced gene 1 protein-like, transcript variant X3
androgen-induced gene 1 protein-like, transcript variant X11
androgen-induced gene 1 protein-like isoform X2
androgen-induced gene 1 protein-like isoform X4
dyslexia-associated protein KIAA0319, transcript variant X1
dyslexia-associated protein KIAA0319, transcript variant X2
dyslexia-associated protein KIAA0319, transcript variant X3
E3 ubiquitin-protein ligase TRIM33-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM33-like, transcript variant X1
E3 ubiquitin-protein ligase TRIM33-like isoform X1
E3 ubiquitin-protein ligase TRIM33-like isoform X2
uncharacterized LOC124956651, transcript variant X3
uncharacterized LOC124956651, transcript variant X2
uncharacterized LOC124956651, transcript variant X1
survival of motor neuron-related-splicing factor 30, transcript variant X1
survival of motor neuron-related-splicing factor 30, transcript variant X2
survival of motor neuron-related-splicing factor 30 isoform X1
survival of motor neuron-related-splicing factor 30 isoform X2
39S ribosomal protein L46, mitochondrial, transcript variant X3
39S ribosomal protein L46, mitochondrial isoform X2
39S ribosomal protein L46, mitochondrial, transcript variant X2
39S ribosomal protein L46, mitochondrial, transcript variant X1
39S ribosomal protein L46, mitochondrial isoform X1
proteasome subunit beta type-1, transcript variant X1
proteasome subunit beta type-1, transcript variant X2
proteasome subunit beta type-1, transcript variant X3
endothelial differentiation-related factor 1 homolog
CCR4-NOT transcription complex subunit 1, transcript variant X2
CCR4-NOT transcription complex subunit 1, transcript variant X1
CCR4-NOT transcription complex subunit 1 isoform X1
CCR4-NOT transcription complex subunit 1 isoform X2
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial, transcript variant X1
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial, transcript variant X4
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial, transcript variant X2
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial, transcript variant X3
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X1
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X2
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial, transcript variant X5
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X3
DNA topoisomerase 3-beta-1, transcript variant X3
DNA topoisomerase 3-beta-1, transcript variant X1
DNA topoisomerase 3-beta-1, transcript variant X2
p21-activated protein kinase-interacting protein 1-like
neprilysin-4-like, transcript variant X2
neprilysin-4-like, transcript variant X1
dipeptidase 1-like, 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 5 samples with support for all annotated introns
dipeptidase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
dipeptidase 1-like, transcript variant X3
dipeptidase 1-like, transcript variant X4
glutamic acid-rich protein-like, transcript variant X2
glutamic acid-rich protein-like, transcript variant X1
glutamic acid-rich protein-like isoform X1
glutamic acid-rich protein-like isoform X2
uncharacterized LOC124956776, transcript variant X3
uncharacterized LOC124956776, transcript variant X1
uncharacterized LOC124956776, transcript variant X2
dynein axonemal heavy chain 7-like, transcript variant X1
dynein axonemal heavy chain 7-like, transcript variant X3
dynein axonemal heavy chain 7-like, transcript variant X2
uncharacterized protein LOC124956776 isoform X1
uncharacterized protein LOC124956776 isoform X2
dynein axonemal heavy chain 7-like isoform X2
dynein axonemal heavy chain 7-like isoform X3
dynein axonemal heavy chain 7-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X3
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X2
probable cleavage and polyadenylation specificity factor subunit 2, transcript variant X1
probable cleavage and polyadenylation specificity factor subunit 2
beclin 1-associated autophagy-related key regulator, transcript variant X2
beclin 1-associated autophagy-related key regulator, transcript variant X3
beclin 1-associated autophagy-related key regulator, transcript variant X1
beclin 1-associated autophagy-related key regulator, transcript variant X4
beclin 1-associated autophagy-related key regulator, transcript variant X5
beclin 1-associated autophagy-related key regulator isoform X1
beclin 1-associated autophagy-related key regulator isoform X2
beclin 1-associated autophagy-related key regulator isoform X3
protein phosphatase 1B, transcript variant X4
protein phosphatase 1B, transcript variant X2
protein phosphatase 1B, transcript variant X3
protein phosphatase 1B, transcript variant X1
mitochondrial import inner membrane translocase subunit Tim23, transcript variant X2
mitochondrial import inner membrane translocase subunit Tim23, transcript variant X3
mitochondrial import inner membrane translocase subunit Tim23, transcript variant X1
mitochondrial import inner membrane translocase subunit Tim23 isoform X2
mitochondrial import inner membrane translocase subunit Tim23 isoform X3
mitochondrial import inner membrane translocase subunit Tim23 isoform X1
AP2-associated protein kinase 1, transcript variant X3
AP2-associated protein kinase 1, transcript variant X2
AP2-associated protein kinase 1, transcript variant X1
AP2-associated protein kinase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
AP2-associated protein kinase 1 isoform X4
AP2-associated protein kinase 1 isoform X3
AP2-associated protein kinase 1 isoform X2
AP2-associated protein kinase 1 isoform X1
snRNA-activating protein complex subunit 4
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
lipase maturation factor 2-like, transcript variant X1
lipase maturation factor 2-like isoform X1
lipase maturation factor 2-like, transcript variant X2
lipase maturation factor 2-like isoform X2
THUMP domain-containing protein 3-like, transcript variant X1
THUMP domain-containing protein 3-like, transcript variant X2
THUMP domain-containing protein 3-like isoform X1
THUMP domain-containing protein 3-like isoform X2
cysteine-rich with EGF-like domain protein 2
transmembrane protein 47, transcript variant X2
transmembrane protein 47, transcript variant X3
transmembrane protein 47, transcript variant X4
transmembrane protein 47, transcript variant X1
chromobox protein homolog 1-like, transcript variant X1
chromobox protein homolog 1-like, transcript variant X2
chromobox protein homolog 1-like isoform X2
chromobox protein homolog 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC124956749, transcript variant X1
uncharacterized protein LOC124956749 isoform X1
uncharacterized LOC124956749, transcript variant X2
uncharacterized protein LOC124956749 isoform X2
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X5
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X5
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X3
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X3
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X4
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X4
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X2
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X1
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X1
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X2
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X6
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X6
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like, transcript variant X7
amyloid beta A4 precursor protein-binding family B member 1-interacting protein-like isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC124956738, transcript variant X3
uncharacterized LOC124956738, transcript variant X2
uncharacterized LOC124956738, transcript variant X1
uncharacterized LOC124956738, transcript variant X4
uncharacterized protein LOC124956738 isoform X1
uncharacterized protein LOC124956738 isoform X2
uncharacterized protein LOC124956738 isoform X3
DNA-directed RNA polymerase II subunit Rpb4-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit Rpb4-like, transcript variant X4
DNA-directed RNA polymerase II subunit Rpb4-like isoform X3
DNA-directed RNA polymerase II subunit Rpb4-like, transcript variant X2
DNA-directed RNA polymerase II subunit Rpb4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit Rpb4-like, transcript variant X3
transcriptional adapter 2-alpha-like isoform X2
transcriptional adapter 2-alpha-like isoform X1
eukaryotic translation initiation factor 3 subunit G
calcium homeostasis endoplasmic reticulum protein, transcript variant X1
calcium homeostasis endoplasmic reticulum protein isoform X1
calcium homeostasis endoplasmic reticulum protein, transcript variant X2
calcium homeostasis endoplasmic reticulum protein, transcript variant X3
calcium homeostasis endoplasmic reticulum protein isoform X2
calcium homeostasis endoplasmic reticulum protein isoform X3
uncharacterized LOC124956691, transcript variant X2
uncharacterized LOC124956691, transcript variant X1
uncharacterized LOC124956669, transcript variant X2
uncharacterized LOC124956669, transcript variant X1
uncharacterized LOC124956669, transcript variant X5
uncharacterized LOC124956669, transcript variant X4
uncharacterized LOC124956669, transcript variant X3
piggyBac transposable element-derived protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein