Diprion similis isolate iyDipSimi1 chromosome 14, iyDipSimi1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Tenthredinoidea; Diprionidae; Diprioninae; Diprion.
REFSEQ INFORMATION: The reference sequence is identical to\nCM037732.1.\nAssembly name: iyDipSimi1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the United States Department of\nAgriculture on 2021/12/10. The original whole-genome shotgun\nproject has the accession JAJNQI000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: United States Department of Agriculture\nAssembly Date :: 17-NOV-2021\nAssembly Method :: HiFiASM v. 0.16.1-r375; Juicebox Assembly\n Toolkit v. 1.11\nAssembly Name :: iyDipSimi1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 100.0x\nSequencing Technology :: PacBio Sequel; Illumina NovaSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Diprion similis Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Catherine Linnen, University of Kentucky
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33% 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 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 3 samples with support for all annotated introns
regulating synaptic membrane exocytosis protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC124414663, 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 15 samples with support for all annotated introns
uncharacterized LOC124414663, 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 64 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 36% 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: 6 Proteins
uncharacterized LOC124414662, transcript variant X2
uncharacterized LOC124414662, transcript variant X1
uncharacterized LOC124414662, transcript variant X3
uncharacterized protein LOC124414662 isoform X3
uncharacterized protein LOC124414662 isoform X1
uncharacterized protein LOC124414662 isoform X2
negative elongation factor A, 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 16 samples with support for all annotated introns
negative elongation factor A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
protein O-GlcNAcase, transcript variant X2
protein O-GlcNAcase, transcript variant X1
28S ribosomal protein S15, mitochondrial
chromatin modification-related protein MEAF6
probable serine/threonine-protein kinase MARK-A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
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 83 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 46% 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 31% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
zinc finger and SCAN domain-containing protein 12-like, transcript variant X3
zinc finger and SCAN domain-containing protein 12-like, transcript variant X1
zinc finger and SCAN domain-containing protein 12-like, transcript variant X2
zinc finger and SCAN domain-containing protein 12-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
protein N-terminal asparagine amidohydrolase, transcript variant X1
protein N-terminal asparagine amidohydrolase, transcript variant X2
protein N-terminal asparagine amidohydrolase
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 19 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 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124414871, transcript variant X2
uncharacterized LOC124414871, transcript variant X1
uncharacterized protein LOC124414871 isoform X2
uncharacterized protein LOC124414871 isoform X1
uncharacterized LOC124414869, 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 4 samples with support for all annotated introns
uncharacterized protein LOC124414869 isoform X2
uncharacterized LOC124414869, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC124414869, transcript variant X3
uncharacterized protein LOC124414869 isoform X1
uncharacterized protein LOC124414869 isoform X3
sodium/potassium/calcium exchanger 1, transcript variant X2
sodium/potassium/calcium exchanger 1, transcript variant X1
uncharacterized protein LOC124414410 isoform X2
sodium/potassium/calcium exchanger 1 isoform X1
28S ribosomal protein S36, mitochondrial
IWS1-like protein, transcript variant X3
IWS1-like protein, transcript variant X2
IWS1-like protein, transcript variant X1
zinc finger protein OZF-like, transcript variant X5
zinc finger protein OZF-like, transcript variant X2
zinc finger protein OZF-like, transcript variant X1
zinc finger protein OZF-like, transcript variant X4
zinc finger protein OZF-like, transcript variant X3
hemolymph lipopolysaccharide-binding protein-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 1 sample with support for all annotated introns
methyltransferase-like protein 22, transcript variant X1
methyltransferase-like protein 22, transcript variant X3
methyltransferase-like protein 22 isoform X1
methyltransferase-like protein 22, transcript variant X2
methyltransferase-like protein 22 isoform X2
methyltransferase-like protein 22 isoform X3
polycomb protein suz12-B, transcript variant X3
polycomb protein suz12-B, transcript variant X2
polycomb protein suz12-B, 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 16 samples with support for all annotated introns
phosphotriesterase-related protein, transcript variant X1
phosphotriesterase-related protein isoform X1
phosphotriesterase-related protein, transcript variant X2
phosphotriesterase-related protein isoform X2
calcium and integrin-binding family member 3
protein IMPACT-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 23 samples with support for all annotated introns
protein IMPACT-like, 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 22 samples with support for all annotated introns
protein IMPACT-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
protein IMPACT-like, 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 32 samples with support for all annotated introns
protein IMPACT-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 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 60% coverage of the annotated genomic feature by RNAseq alignments
WD repeat-containing protein CG11141, transcript variant X1
WD repeat-containing protein CG11141, transcript variant X3
WD repeat-containing protein CG11141, 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 1 sample with support for all annotated introns
uncharacterized LOC124414930, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
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 31 samples with support for all annotated introns
uncharacterized LOC124414930, 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 41 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 1 sample with support for all annotated introns
serine/threonine-protein kinase Genghis Khan, transcript variant X5
serine/threonine-protein kinase Genghis Khan, transcript variant X1
serine/threonine-protein kinase Genghis Khan, 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 MRCK beta isoform X2
serine/threonine-protein kinase Genghis Khan isoform X1
deubiquitinase DESI2, 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 12 samples with support for all annotated introns
deubiquitinase DESI2, 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 1 sample with support for all annotated introns
deubiquitinase DESI2, 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 36 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
probable ATP-dependent RNA helicase DHX35
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
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 57 samples with support for all annotated introns
uncharacterized LOC124414937, transcript variant X2
uncharacterized LOC124414937, 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 50 samples with support for all annotated introns
oxysterol-binding protein-related protein 9, transcript variant X1
oxysterol-binding protein-related protein 9, transcript variant X2
oxysterol-binding protein-related protein 9 isoform X1
oxysterol-binding protein-related protein 9 isoform X2
oxysterol-binding protein-related protein 9, transcript variant X3
elongation of very long chain fatty acids protein AAEL008004-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 28 samples with support for all annotated introns
oxysterol-binding protein-related protein 9 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
U6 snRNA-associated Sm-like protein LSm6
very long-chain-fatty-acid--CoA ligase bubblegum, transcript variant X2
very long-chain-fatty-acid--CoA ligase bubblegum, transcript variant X1
very long-chain-fatty-acid--CoA ligase bubblegum isoform X1
very long-chain-fatty-acid--CoA ligase bubblegum isoform X2
m-AAA protease-interacting protein 1, mitochondrial-like
mucosa-associated lymphoid tissue lymphoma translocation protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
CREB-regulated transcription coactivator 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CREB-regulated transcription coactivator 1-like, transcript variant X2
CREB-regulated transcription coactivator 1-like, transcript variant X7
CREB-regulated transcription coactivator 1-like, 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 2 samples with support for all annotated introns
CREB-regulated transcription coactivator 1-like, transcript variant X4
CREB-regulated transcription coactivator 1-like, transcript variant X6
CREB-regulated transcription coactivator 1-like, transcript variant X8
CREB-regulated transcription coactivator 1-like, transcript variant X9
CREB-regulated transcription coactivator 1-like, transcript variant X3
CREB-regulated transcription coactivator 1-like isoform X1
CREB-regulated transcription coactivator 1-like isoform X2
CREB-regulated transcription coactivator 1-like isoform X7
CREB-regulated transcription coactivator 1-like isoform X5
CREB-regulated transcription coactivator 1-like isoform X4
CREB-regulated transcription coactivator 1-like isoform X6
CREB-regulated transcription coactivator 1-like isoform X8
CREB-regulated transcription coactivator 1-like isoform X9
CREB-regulated transcription coactivator 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
microsomal glutathione S-transferase 1-like
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
uncharacterized LOC124414653, transcript variant X2
uncharacterized LOC124414653, transcript variant X3
uncharacterized LOC124414653, 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
IQ and ubiquitin-like domain-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: IQ and ubiquitin-like domain-containing protein
N-alpha-acetyltransferase 35, NatC auxiliary subunit
inositol polyphosphate 5-phosphatase OCRL, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
inositol polyphosphate 5-phosphatase OCRL, 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 9 samples with support for all annotated introns
inositol polyphosphate 5-phosphatase OCRL isoform X1
inositol polyphosphate 5-phosphatase OCRL isoform X2
importin subunit alpha, transcript variant X1
importin subunit alpha, transcript variant X2
importin subunit alpha, transcript variant X3
vesicle transport protein SFT2A, transcript variant X3
vesicle transport protein SFT2A, transcript variant X1
vesicle transport protein SFT2A, transcript variant X2
vesicle transport protein SFT2A isoform X2
vesicle transport protein SFT2A isoform X1
uncharacterized LOC124414648, 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
uncharacterized LOC124414648, 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 50 samples with support for all annotated introns
uncharacterized LOC124414648, 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 67 samples with support for all annotated introns
DNA repair protein complementing XP-A cells homolog, transcript variant X2
DNA repair protein complementing XP-A cells homolog, transcript variant X1
DNA repair protein complementing XP-A cells homolog isoform X2
DNA repair protein complementing XP-A cells homolog isoform X1
3-hydroxy-3-methylglutaryl-coenzyme A reductase, transcript variant X1
3-hydroxy-3-methylglutaryl-coenzyme A reductase, transcript variant X2
3-hydroxy-3-methylglutaryl-coenzyme A reductase, transcript variant X3
3-hydroxy-3-methylglutaryl-coenzyme A reductase
protein phosphatase methylesterase 1, transcript variant X2
protein phosphatase methylesterase 1, transcript variant X1
protein phosphatase methylesterase 1 isoform X2
protein phosphatase methylesterase 1 isoform X1
retinoblastoma-binding protein 5 homolog
jerky protein homolog-like, transcript variant X3
jerky protein homolog-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 8 samples with support for all annotated introns
jerky protein homolog-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
spectrin beta chain, non-erythrocytic 1, transcript variant X8
spectrin beta chain, non-erythrocytic 1, transcript variant X4
spectrin beta chain, non-erythrocytic 1, transcript variant X7
spectrin beta chain, non-erythrocytic 1, transcript variant X2
spectrin beta chain, non-erythrocytic 1, transcript variant X3
spectrin beta chain, non-erythrocytic 1, transcript variant X6
spectrin beta chain, non-erythrocytic 1, transcript variant X5
spectrin beta chain, non-erythrocytic 1, transcript variant X1
spectrin beta chain, non-erythrocytic 1 isoform X4
spectrin beta chain, non-erythrocytic 1 isoform X7
spectrin beta chain, non-erythrocytic 1 isoform X2
spectrin beta chain, non-erythrocytic 1 isoform X3
spectrin beta chain, non-erythrocytic 1 isoform X6
spectrin beta chain, non-erythrocytic 1 isoform X5
spectrin beta chain, non-erythrocytic 1 isoform X1
spectrin beta chain, non-erythrocytic 1 isoform X8
endoribonuclease Dicer, transcript variant X2
endoribonuclease Dicer, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 87% 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.
mitochondrial import receptor subunit TOM20 homolog
porphobilinogen deaminase, transcript variant X2
porphobilinogen deaminase, transcript variant X3
porphobilinogen deaminase, transcript variant X1
general transcription and DNA repair factor IIH helicase subunit XPD, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
BRO1 domain-containing protein BROX-like
lactoylglutathione lyase, 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 73 samples with support for all annotated introns
lactoylglutathione lyase, 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 55 samples with support for all annotated introns
tubulin-specific chaperone E, transcript variant X1
tubulin-specific chaperone E, transcript variant X2
general transcription and DNA repair factor IIH helicase subunit XPD, 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 6 samples with support for all annotated introns
general transcription and DNA repair factor IIH helicase subunit XPD, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
general transcription and DNA repair factor IIH helicase subunit XPD isoform X1
general transcription and DNA repair factor IIH helicase subunit XPD isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 94% coverage of the annotated genomic feature by RNAseq alignments
cofilin/actin-depolymerizing factor homolog
actin-related protein 2, transcript variant X3
actin-related protein 2, transcript variant X2
actin-related protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
gustatory receptor for bitter taste 66a-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
limbic system-associated membrane protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 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 94% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC124414514
cysteine-rich hydrophobic domain-containing protein 2, 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 14 samples with support for all annotated introns
cysteine-rich hydrophobic domain-containing protein 2, 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 51 samples with support for all annotated introns
cysteine-rich hydrophobic domain-containing protein 2 isoform X2
cysteine-rich hydrophobic domain-containing protein 2 isoform 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 77 samples with support for all annotated introns
amino acid transporter AVT1C, 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 1 sample with support for all annotated introns
amino acid transporter AVT1C, 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 1 sample with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB1 isoform X2
DNA-directed RNA polymerase II subunit RPB1 isoform X1
heterogeneous nuclear ribonucleoprotein H-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
MOB kinase activator 1B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
MOB kinase activator 1B, transcript variant X1
sodium- and chloride-dependent glycine transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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 40 samples with support for all annotated introns
lymphocyte antigen 75-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 22 samples with support for all annotated introns
lymphocyte antigen 75-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 31 samples with support for all annotated introns
uncharacterized protein LOC124414576 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zwei Ig domain protein zig-8, transcript variant X1
zwei Ig domain protein zig-8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
maternal protein exuperantia, transcript variant X1
maternal protein exuperantia, 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 74 samples with support for all annotated introns
acetyl-CoA acetyltransferase, mitochondrial
sodium-dependent transporter bedraggled, transcript variant X6
sodium-dependent transporter bedraggled, transcript variant X1
sodium-dependent transporter bedraggled, transcript variant X3
sodium-dependent transporter bedraggled, transcript variant X4
sodium-dependent transporter bedraggled, transcript variant X5
sodium-dependent transporter bedraggled, transcript variant X2
sodium-dependent transporter bedraggled isoform X1
sodium-dependent transporter bedraggled isoform X3
sodium-dependent transporter bedraggled isoform X4
sodium-dependent transporter bedraggled isoform X5
sodium-dependent transporter bedraggled isoform X2
sodium- and chloride-dependent glycine transporter 2 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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
SHC-transforming protein 1, transcript variant X3
SHC-transforming protein 1, transcript variant X1
SHC-transforming protein 1, transcript variant X2
MIP18 family protein galla-1, 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 31 samples with support for all annotated introns
MIP18 family protein galla-1, 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 81 samples with support for all annotated introns
baculoviral IAP repeat-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
DNA mismatch repair protein Msh2, transcript variant X1
DNA mismatch repair protein Msh2, transcript variant X2
DNA mismatch repair protein Msh2 isoform X1
DNA mismatch repair protein Msh2 isoform X2
uncharacterized LOC124414977, transcript variant X2
uncharacterized LOC124414977, transcript variant X1
uncharacterized protein LOC124414977 isoform X2
uncharacterized protein LOC124414977 isoform X1
uncharacterized LOC124414990, transcript variant X1
uncharacterized LOC124414990, transcript variant X2
uncharacterized LOC124414990, 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 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 30 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 7 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 15 samples with support for all annotated introns
actin-related protein 2-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 11 samples with support for all annotated introns
actin-related protein 2-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 30 samples with support for all annotated introns
adenylyltransferase and sulfurtransferase MOCS3
probable galactose-1-phosphate uridylyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable galactose-1-phosphate uridylyltransferase, transcript variant X4
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 46 samples with support for all annotated introns
probable galactose-1-phosphate uridylyltransferase, transcript variant X3
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
probable galactose-1-phosphate uridylyltransferase, transcript variant X1
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 8 samples with support for all annotated introns
probable galactose-1-phosphate uridylyltransferase isoform X3
probable galactose-1-phosphate uridylyltransferase isoform X2
probable galactose-1-phosphate uridylyltransferase isoform X1
probable small nuclear ribonucleoprotein Sm D2, transcript variant X1
probable small nuclear ribonucleoprotein Sm D2, transcript variant X2
probable small nuclear ribonucleoprotein Sm D2 isoform X1
probable small nuclear ribonucleoprotein Sm D2 isoform X2
trafficking protein particle complex subunit 13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
chromodomain-helicase-DNA-binding protein 1
saccharopine dehydrogenase-like oxidoreductase
GTP cyclohydrolase 1, 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 9 samples with support for all annotated introns
GTP cyclohydrolase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized LOC124414854, transcript variant X2
uncharacterized protein LOC124414854 isoform X2
uncharacterized LOC124414854, transcript variant X1
uncharacterized protein LOC124414854 isoform X1
rRNA 2'-O-methyltransferase fibrillarin, transcript variant X1
rRNA 2'-O-methyltransferase fibrillarin, transcript variant X2
rRNA 2'-O-methyltransferase fibrillarin isoform X2
rRNA 2'-O-methyltransferase fibrillarin isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 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
irregular chiasm C-roughest protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
FERM domain-containing protein 5, transcript variant X2
FERM domain-containing protein 5, transcript variant X5
FERM domain-containing protein 5, transcript variant X4
FERM domain-containing protein 5, transcript variant X3
FERM domain-containing protein 5, transcript variant X1
FERM domain-containing protein 5 isoform X2
FERM domain-containing protein 5 isoform X5
FERM domain-containing protein 5 isoform X4
FERM domain-containing protein 5 isoform X3
FERM domain-containing protein 5 isoform X1
iron-sulfur cluster co-chaperone protein HscB
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 40 samples with support for all annotated introns
Golgi membrane protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Golgi membrane protein 1-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 35 samples with support for all annotated introns
uncharacterized protein LOC124414834 isoform X3
Golgi membrane protein 1-like isoform X1
Golgi membrane protein 1-like, transcript variant X2
uncharacterized protein LOC124414834 isoform X2
odorant receptor Or1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
odorant receptor Or1-like, transcript variant X1
thrombospondin type-1 domain-containing protein 4-like
armadillo repeat-containing protein 6 homolog
dynein heavy chain, cytoplasmic, 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 9 samples with support for all annotated introns
dynein heavy chain, cytoplasmic, 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 9 samples with support for all annotated introns
dynein heavy chain, cytoplasmic, 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 13 samples with support for all annotated introns
dynein heavy chain, cytoplasmic, transcript variant X4
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
dynein heavy chain, cytoplasmic, transcript variant X8
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
dynein heavy chain, cytoplasmic, 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 12 samples with support for all annotated introns
dynein heavy chain, cytoplasmic, 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 20 samples with support for all annotated introns
dynein heavy chain, cytoplasmic, transcript variant X6
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 20 samples with support for all annotated introns
dynein heavy chain, cytoplasmic isoform X2
dynein heavy chain, cytoplasmic isoform X1
dynein heavy chain, cytoplasmic isoform X5
dynein heavy chain, cytoplasmic isoform X4
dynein heavy chain, cytoplasmic isoform X8
dynein heavy chain, cytoplasmic isoform X3
dynein heavy chain, cytoplasmic isoform X7
dynein heavy chain, cytoplasmic isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
hemolymph lipopolysaccharide-binding protein-like, transcript variant X2
hemolymph lipopolysaccharide-binding protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
methylthioribulose-1-phosphate dehydratase
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 78 samples with support for all annotated introns
CWF19-like protein 1, transcript variant X2
CWF19-like protein 1, transcript variant X1
protein single-minded, 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
protein single-minded, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
c-Myc-binding protein, 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 59 samples with support for all annotated introns
c-Myc-binding protein, transcript variant X2
proto-oncogene tyrosine-protein kinase ROS, transcript variant X1
proto-oncogene tyrosine-protein kinase ROS, transcript variant X2
proto-oncogene tyrosine-protein kinase ROS, transcript variant X3
proto-oncogene tyrosine-protein kinase ROS, transcript variant X4
proto-oncogene tyrosine-protein kinase ROS, transcript variant X6
proto-oncogene tyrosine-protein kinase ROS, transcript variant X5
proto-oncogene tyrosine-protein kinase ROS isoform X1
proto-oncogene tyrosine-protein kinase ROS isoform X5
proto-oncogene tyrosine-protein kinase ROS isoform X2
proto-oncogene tyrosine-protein kinase ROS isoform X3
proto-oncogene tyrosine-protein kinase ROS isoform X4
proto-oncogene tyrosine-protein kinase ROS isoform X6
cAMP-dependent protein kinase catalytic subunit 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
FHA domain-containing protein DDL-like, transcript variant X2
FHA domain-containing protein DDL-like, transcript variant X1
molybdenum cofactor biosynthesis protein 1, 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 30 samples with support for all annotated introns
molybdenum cofactor biosynthesis protein 1 isoform X1
molybdenum cofactor biosynthesis protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
molybdenum cofactor biosynthesis protein 1 isoform X2
kelch-like protein 5, 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 14 samples with support for all annotated introns
kelch-like protein 5, 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 9 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 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: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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: 50 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
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 47 samples with support for all annotated introns
DNA damage-regulated autophagy modulator protein 2-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 71 samples with support for all annotated introns
uncharacterized protein LOC124414968 isoform X1
DNA damage-regulated autophagy modulator protein 2-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 1 sample with support for all annotated introns
DNA damage-regulated autophagy modulator protein 2-like isoform X2
DNA damage-regulated autophagy modulator protein 2-like
monocarboxylate transporter 10-like, transcript variant X1
monocarboxylate transporter 10-like, transcript variant X2
monocarboxylate transporter 10-like isoform X1
monocarboxylate transporter 12-like isoform X2
glutamate receptor ionotropic, kainate 2-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
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.
glutamate receptor ionotropic, kainate 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate receptor ionotropic, kainate 2
glutamate receptor ionotropic, kainate 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
palmitoleoyl-protein carboxylesterase NOTUM
PI-PLC X domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 94% 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: 82 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential channel pyrexia
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
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 63 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 85 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 44 samples with support for all annotated introns
probable 28S ribosomal protein S6, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DNA methyltransferase 1-associated protein 1
major facilitator superfamily domain-containing protein 12-like
rho guanine nucleotide exchange factor 11, transcript variant X1
rho guanine nucleotide exchange factor 11, transcript variant X2
rho guanine nucleotide exchange factor 11, transcript variant X4
rho guanine nucleotide exchange factor 11, transcript variant X6
rho guanine nucleotide exchange factor 11 isoform X1
rho guanine nucleotide exchange factor 11 isoform X2
rho guanine nucleotide exchange factor 12 isoform X4
rho guanine nucleotide exchange factor 11 isoform X6
rho guanine nucleotide exchange factor 11, transcript variant X5
rho guanine nucleotide exchange factor 11 isoform X5
rho guanine nucleotide exchange factor 11, transcript variant X3
rho guanine nucleotide exchange factor 11 isoform X3
28S ribosomal protein S29, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 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 14 samples with support for all annotated introns
ankyrin repeat and KH domain-containing protein mask-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 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 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 90% coverage of the annotated genomic feature by RNAseq alignments
probable U3 small nucleolar RNA-associated protein 11, 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 19 samples with support for all annotated introns
probable U3 small nucleolar RNA-associated protein 11, 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 8 samples with support for all annotated introns
probable U3 small nucleolar RNA-associated protein 11, 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 32 samples with support for all annotated introns
probable U3 small nucleolar RNA-associated protein 11, 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 30 samples with support for all annotated introns
probable U3 small nucleolar RNA-associated protein 11
transient receptor potential cation channel trpm, 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 3 samples with support for all annotated introns
transient receptor potential cation channel trpm, transcript variant X5
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
transient receptor potential cation channel trpm, transcript variant X4
transient receptor potential cation channel trpm, transcript variant X7
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
transient receptor potential cation channel trpm, transcript variant X3
transient receptor potential cation channel trpm, transcript variant X6
transient receptor potential cation channel trpm, transcript variant X2
transient receptor potential cation channel trpm isoform X2
transient receptor potential cation channel trpm isoform X5
transient receptor potential cation channel trpm isoform X1
transient receptor potential cation channel trpm isoform X4
transient receptor potential cation channel trpm isoform X3
transient receptor potential cation channel trpm isoform 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 1 sample 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 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: 84 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC124414466
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 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84 Proteins, and 96% 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 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC124414467
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 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: 78 Proteins, and 91% 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: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 samples with support for all annotated introns
cytochrome P450 6a2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 80 samples with support for all annotated introns
cytochrome P450 6a2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
cytochrome P450 6A1-like, transcript variant X2
cytochrome P450 6A1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: odorant receptor 82a-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
ADAMTS-like protein 4, transcript variant X2
ADAMTS-like protein 4, 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 4 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 86 samples with support for all annotated introns
probable cytochrome P450 6a14, transcript variant X1
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 81 samples with support for all annotated introns
probable cytochrome P450 6a14 isoform X1
probable cytochrome P450 6a14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
probable cytochrome P450 6a14 isoform X2
cell division cycle protein 27 homolog, transcript variant X3
cell division cycle protein 27 homolog, transcript variant X2
cell division cycle protein 27 homolog, transcript variant X1
cell division cycle protein 27 homolog isoform X3
cell division cycle protein 27 homolog isoform X2
cell division cycle protein 27 homolog isoform X1
uncharacterized protein C20orf85 homolog
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 15 samples with support for all annotated introns
leukocyte receptor cluster member 1 homolog
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
U3 small nucleolar RNA-associated protein 4 homolog
chromosome transmission fidelity protein 8 homolog
type 1 phosphatidylinositol 4,5-bisphosphate 4-phosphatase, 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 48 samples with support for all annotated introns
type 1 phosphatidylinositol 4,5-bisphosphate 4-phosphatase, 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 82 samples with support for all annotated introns
type 1 phosphatidylinositol 4,5-bisphosphate 4-phosphatase isoform X1
type 2 phosphatidylinositol 4,5-bisphosphate 4-phosphatase isoform X2
eukaryotic translation initiation factor 3 subunit E
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-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 3 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 79% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
LOW QUALITY PROTEIN: 15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% 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 4 samples with support for all annotated introns
uncharacterized LOC124414735, 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 LOC124414735, transcript variant X2
uncharacterized LOC124414735, transcript variant X3
uncharacterized LOC124414735, transcript variant X4
uncharacterized protein LOC124414735 isoform X1
uncharacterized protein LOC124414735 isoform X3
uncharacterized protein LOC124414735 isoform X2
uncharacterized protein LOC124414735 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124414827, transcript variant X2
uncharacterized LOC124414827, transcript variant X1
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 3 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 27% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124414726, transcript variant X1
uncharacterized LOC124414726, transcript variant X2
uncharacterized protein LOC124414726 isoform X1
uncharacterized protein LOC124414726 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized protein LOC124414849 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% 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 74% coverage of the annotated genomic feature by RNAseq alignments
non-lysosomal glucosylceramidase, 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 5 samples with support for all annotated introns
non-lysosomal glucosylceramidase, transcript variant X2
ciliogenesis and planar polarity effector 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 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 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 78 samples with support for all annotated introns
protein lethal(2)essential for life-like
uncharacterized MFS-type transporter C09D4.1-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 9 samples with support for all annotated introns
feline leukemia virus subgroup C receptor-related protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 94% 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 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
feline leukemia virus subgroup C receptor-related protein 2-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 3 samples with support for all annotated introns
feline leukemia virus subgroup C receptor-related protein 2-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 13 samples with support for all annotated introns
feline leukemia virus subgroup C receptor-related protein 2-like, 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 13 samples with support for all annotated introns
feline leukemia virus subgroup C receptor-related protein 2-like isoform X1
feline leukemia virus subgroup C receptor-related protein 2-like isoform X2
feline leukemia virus subgroup C receptor-related protein 2-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
geranylgeranyl transferase type-2 subunit beta
testis-specific serine/threonine-protein kinase 4-like
glycerol kinase-like, transcript variant X1
glycerol kinase-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 26 samples with support for all annotated introns
uncharacterized LOC124414507, transcript variant X3
uncharacterized LOC124414507, transcript variant X2
uncharacterized LOC124414507, transcript variant X1
rho guanine nucleotide exchange factor 10-like protein, transcript variant X1
rho guanine nucleotide exchange factor 10-like protein, transcript variant X2
rho guanine nucleotide exchange factor 10-like protein, transcript variant X3
rho guanine nucleotide exchange factor 10-like protein, transcript variant X5
rho guanine nucleotide exchange factor 10-like protein, transcript variant X4
rho guanine nucleotide exchange factor 10-like protein, transcript variant X6
rho guanine nucleotide exchange factor 10-like protein isoform X1
rho guanine nucleotide exchange factor 10-like protein isoform X2
rho guanine nucleotide exchange factor 10-like protein isoform X3
uncharacterized protein LOC124414506 isoform X5
rho guanine nucleotide exchange factor 10-like protein isoform X4
rho guanine nucleotide exchange factor 10-like protein isoform X6
uncharacterized LOC124414529, transcript variant X3
uncharacterized LOC124414529, 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 18 samples with support for all annotated introns
uncharacterized LOC124414529, 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 38 samples with support for all annotated introns
uncharacterized protein LOC124414529 isoform X3
uncharacterized protein LOC124414529 isoform X1
uncharacterized protein LOC124414529 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 2 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 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
polyglutamine-repeat protein pqn-41-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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: 4 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments, including 40 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transfer RNA phenylalanine (anticodon GAA); 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RNA-binding protein 25, transcript variant X1
zinc finger protein 300-like, transcript variant X2
zinc finger protein 300-like, transcript variant X1
zinc finger protein 300-like, transcript variant X3
RNA-binding protein 25, 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
B9 domain-containing protein 2-like, transcript variant X1
B9 domain-containing protein 2-like, transcript variant X3
B9 domain-containing protein 2-like, transcript variant X2
B9 domain-containing protein 2-like isoform X2
B9 domain-containing protein 2-like, transcript variant X4
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
B9 domain-containing protein 2-like isoform X1
B9 domain-containing protein 2-like isoform X3
pleckstrin homology domain-containing family F member 2
serine/threonine-protein kinase VRK1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
LOW QUALITY PROTEIN: serine/threonine-protein kinase VRK1-like
uncharacterized LOC124414743, transcript variant X1
uncharacterized LOC124414743, 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
uncharacterized protein LOC124414743 isoform X1
uncharacterized protein LOC124414743 isoform X2
uncharacterized LOC124414743, 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 11 samples with support for all annotated introns
uncharacterized protein LOC124414743 isoform X3
PAX3- and PAX7-binding protein 1, transcript variant X1
PAX3- and PAX7-binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
PAX3- and PAX7-binding protein 1 isoform X1
PAX3- and PAX7-binding protein 1 isoform X2
uncharacterized LOC124414744, transcript variant X2
uncharacterized LOC124414744, transcript variant X1
uncharacterized LOC124414744, transcript variant X3
uncharacterized protein LOC124414744 isoform X1
uncharacterized protein LOC124414744 isoform X2
dehydrodolichyl diphosphate synthase complex subunit DHDDS, transcript variant X1
dehydrodolichyl diphosphate synthase complex subunit DHDDS, transcript variant X2
dehydrodolichyl diphosphate synthase complex subunit DHDDS
PH-interacting protein, transcript variant X1
PH-interacting protein, transcript variant X2
PH-interacting protein, transcript variant X3
dystrophin, isoforms A/C/F/G/H, transcript variant X1
dystrophin, isoforms A/C/F/G/H, transcript variant X2
dystrophin, isoforms A/C/F/G/H isoform X1
dystrophin, isoforms A/C/F/G/H isoform X2
NKG2-E type II integral membrane protein-like
H/ACA ribonucleoprotein complex subunit 3
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
trafficking protein particle complex subunit 10, transcript variant X1
trafficking protein particle complex subunit 10, transcript variant X3
trafficking protein particle complex subunit 10, transcript variant X4
trafficking protein particle complex subunit 10, transcript variant X2
trafficking protein particle complex subunit 10
prostaglandin E2 receptor EP2 subtype, transcript variant X2
prostaglandin E2 receptor EP2 subtype, 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
prostaglandin E2 receptor EP2 subtype isoform X2
prostaglandin E2 receptor EP2 subtype isoform X1
uncharacterized LOC124414754, transcript variant X1
uncharacterized LOC124414754, transcript variant X2
uncharacterized protein LOC124414754 isoform X1
uncharacterized protein LOC124414754 isoform X2
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-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 29 samples with support for all annotated introns
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-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 8 samples with support for all annotated introns
protein LSM14 homolog B, transcript variant X1
protein LSM14 homolog B, transcript variant X3
protein LSM14 homolog B, transcript variant X2
cytochrome c1, heme protein, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 149 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: beta-1,3-glucan-binding protein 1-like
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like isoform X1
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC124414701 isoform X1
uncharacterized protein LOC124414701 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
hemolymph lipopolysaccharide-binding protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 50 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 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 97% 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: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peroxisomal hydratase-dehydrogenase-epimerase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 96% 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
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 1 sample with support for all annotated introns
28S ribosomal protein S9, mitochondrial-like, transcript variant X2
28S ribosomal protein S9, mitochondrial-like isoform X2
28S ribosomal protein S9, mitochondrial-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 28 samples with support for all annotated introns
transient receptor potential channel pyrexia-like isoform X1
probable arginine--tRNA ligase, mitochondrial
phosphatidylinositol-binding clathrin assembly protein unc-11, transcript variant X6
phosphatidylinositol-binding clathrin assembly protein unc-11, transcript variant X1
phosphatidylinositol-binding clathrin assembly protein unc-11, transcript variant X2
phosphatidylinositol-binding clathrin assembly protein unc-11, transcript variant X5
phosphatidylinositol-binding clathrin assembly protein unc-11, transcript variant X3
phosphatidylinositol-binding clathrin assembly protein unc-11, transcript variant X7
phosphatidylinositol-binding clathrin assembly protein unc-11, transcript variant X4
phosphatidylinositol-binding clathrin assembly protein unc-11, transcript variant X9
phosphatidylinositol-binding clathrin assembly protein unc-11, transcript variant X8
phosphatidylinositol-binding clathrin assembly protein unc-11 isoform X1
phosphatidylinositol-binding clathrin assembly protein unc-11 isoform X8
phosphatidylinositol-binding clathrin assembly protein unc-11 isoform X9
phosphatidylinositol-binding clathrin assembly protein unc-11 isoform X2
phosphatidylinositol-binding clathrin assembly protein isoform X5
phosphatidylinositol-binding clathrin assembly protein unc-11 isoform X3
phosphatidylinositol-binding clathrin assembly protein isoform X7
phosphatidylinositol-binding clathrin assembly protein unc-11 isoform X6
phosphatidylinositol-binding clathrin assembly protein unc-11 isoform 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 73 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
28S ribosomal protein S11, mitochondrial
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
28S ribosomal protein S17, mitochondrial
RNA polymerase II subunit A C-terminal domain phosphatase
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 25 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 49 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 69 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 66 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 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 65% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
lisH domain-containing protein ARMC9-like, transcript variant X2
lisH domain-containing protein ARMC9-like, transcript variant X1
lisH domain-containing protein ARMC9-like isoform X2
uncharacterized protein LOC124414891 isoform X1
lisH domain-containing protein ARMC9-like, transcript variant X3
lisH domain-containing protein ARMC9-like isoform X3
alpha-ketoglutarate-dependent dioxygenase alkB homolog 6
THO complex subunit 7 homolog, transcript variant X2
THO complex subunit 7 homolog isoform X2
THO complex subunit 7 homolog, transcript variant X1
THO complex subunit 7 homolog isoform X1
zinc finger protein ubi-d4 A, transcript variant X1
zinc finger protein ubi-d4 A, transcript variant X3
zinc finger protein ubi-d4 A, transcript variant X2
zinc finger protein ubi-d4 A, transcript variant X4
iodotyrosine deiodinase 1, transcript variant X1
iodotyrosine deiodinase 1, transcript variant X2
ribosomal protein S6 kinase alpha-5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
ribosomal protein S6 kinase alpha-5-like isoform X2
ribosomal protein S6 kinase alpha-5-like, transcript variant X1
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 1 sample with support for all annotated introns
ribosomal protein S6 kinase alpha-5-like isoform X1
methyltransferase-like protein 25B, transcript variant X2
methyltransferase-like protein 25B, transcript variant X1
methyltransferase-like protein 25B isoform X2
methyltransferase-like protein 25B isoform X1
tRNA (guanine-N(7)-)-methyltransferase non-catalytic subunit wdr4
lysophosphatidylserine lipase ABHD12, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
lysophosphatidylserine lipase ABHD12, 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 3 samples with support for all annotated introns
lysophosphatidylserine lipase ABHD12, transcript variant X6
lysophosphatidylserine lipase ABHD12, transcript variant X5
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
lysophosphatidylserine lipase ABHD12 isoform X5
lysophosphatidylserine lipase ABHD12 isoform X3
lysophosphatidylserine lipase ABHD12 isoform X4
lysophosphatidylserine lipase ABHD12, transcript variant X1
lysophosphatidylserine lipase ABHD12, 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 43 samples with support for all annotated introns
lysophosphatidylserine lipase ABHD12 isoform X1
lysophosphatidylserine lipase ABHD12 isoform X2
lysophosphatidylserine lipase ABHD12, transcript variant X8
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
lysophosphatidylserine lipase ABHD12, transcript variant X7
lysophosphatidylserine lipase ABHD12 isoform X7
lysophosphatidylserine lipase ABHD12 isoform X6
insulin-like receptor, transcript variant X3
insulin-like receptor, transcript variant X1
insulin-like receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
probable 39S ribosomal protein L24, mitochondrial
calcium uptake protein 2, mitochondrial-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 25 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 81% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
dynein light chain Tctex-type 1, transcript variant X5
dynein light chain Tctex-type 1 isoform X4
dynein light chain Tctex-type 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 8 samples with support for all annotated introns
dynein light chain Tctex-type 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
dynein light chain Tctex-type 1, transcript variant X3
dynein light chain Tctex-type 1, transcript variant X2
distal membrane-arm assembly complex protein 2
U11/U12 small nuclear ribonucleoprotein 25 kDa protein isoform X1
U11/U12 small nuclear ribonucleoprotein 25 kDa protein isoform X2
U11/U12 small nuclear ribonucleoprotein 25 kDa protein isoform X3
histone-lysine N-methyltransferase trithorax
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 11 samples with support for all annotated introns
protein capicua homolog, transcript variant X4
protein capicua homolog, transcript variant X2
protein capicua homolog, transcript variant X11
protein capicua homolog, transcript variant X6
protein capicua homolog, transcript variant X10
protein capicua homolog, transcript variant X9
protein capicua homolog, transcript variant X1
protein capicua homolog, transcript variant X7
protein capicua homolog, transcript variant X14
protein capicua homolog, transcript variant X13
protein capicua homolog, transcript variant X12
protein capicua homolog, transcript variant X5
protein capicua homolog, transcript variant X8
protein capicua homolog, transcript variant X3
GRIP and coiled-coil domain-containing protein 1, transcript variant X3
GRIP and coiled-coil domain-containing protein 1, transcript variant X2
GRIP and coiled-coil domain-containing protein 1, transcript variant X1
GRIP and coiled-coil domain-containing protein 1, transcript variant X4
GRIP and coiled-coil domain-containing protein 1 isoform X3
GRIP and coiled-coil domain-containing protein 1 isoform X2
GRIP and coiled-coil domain-containing protein 1 isoform X1
centrosomal protein of 152 kDa-like, transcript variant X2
centrosomal protein of 152 kDa-like, transcript variant X1
centrosomal protein of 152 kDa-like isoform X1
centrosomal protein of 152 kDa-like isoform X2
lysosomal Pro-X carboxypeptidase, transcript variant X1
lysosomal Pro-X carboxypeptidase, transcript variant X2
lysosomal Pro-X carboxypeptidase isoform X1
lysosomal Pro-X carboxypeptidase isoform X2
kinesin-like protein KIF3A, transcript variant X2
kinesin-like protein KIF3A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology-like domain family B member 1
zinc finger matrin-type protein 5, 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 29 samples with support for all annotated introns
zinc finger matrin-type protein 5, 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 70 samples with support for all annotated introns
cilia- and flagella-associated protein 91, transcript variant X1
cilia- and flagella-associated protein 91, transcript variant X2
cilia- and flagella-associated protein 91 isoform X2
uncharacterized protein LOC124415016 isoform X1
arrestin domain-containing protein 2, transcript variant X2
arrestin domain-containing protein 2, transcript variant X1
arrestin domain-containing protein 2, transcript variant X3
arrestin domain-containing protein 2 isoform X1
arrestin domain-containing protein 2 isoform X2
UPF0235 protein C15orf40 homolog, transcript variant X2
UPF0235 protein C15orf40 homolog, transcript variant X1
coiled-coil domain-containing protein 124
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 62 samples with support for all annotated introns
uncharacterized LOC124415011, 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 4 samples with support for all annotated introns
uncharacterized LOC124415011, transcript variant X1
uncharacterized LOC124415011, 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 13 samples with support for all annotated introns
E3 ubiquitin-protein ligase LNX-like, transcript variant X2
E3 ubiquitin-protein ligase LNX-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
E3 ubiquitin-protein ligase LNX-like isoform X2
E3 ubiquitin-protein ligase LNX-like isoform 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 8 samples with support for all annotated introns
cilia- and flagella-associated protein 298, transcript variant X5
cilia- and flagella-associated protein 298 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
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 54 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
uncharacterized LOC124414908, transcript variant X2
uncharacterized LOC124414908, transcript variant X1
cilia- and flagella-associated protein 298, transcript variant X2
cilia- and flagella-associated protein 298, transcript variant X3
cilia- and flagella-associated protein 298, transcript variant X1
cilia- and flagella-associated protein 298, transcript variant X4
hrp65 protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
hrp65 protein-like, transcript variant X1
hrp65 protein-like, 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
protein eva-1 homolog C-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 10 samples with support for all annotated introns
protein eva-1 homolog C-like, transcript variant X3
protein eva-1 homolog C-like, 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 8 samples with support for all annotated introns
protein eva-1 homolog C-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 21 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 8 samples with support for all annotated introns
RNA polymerase-associated protein CTR9 homolog, transcript variant X1
RNA polymerase-associated protein CTR9 homolog, transcript variant X2
RNA polymerase-associated protein CTR9 homolog isoform X1
RNA polymerase-associated protein CTR9 homolog isoform X2
WD repeat and HMG-box DNA-binding protein 1, transcript variant X1
WD repeat and HMG-box DNA-binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
WD repeat and HMG-box DNA-binding protein 1 isoform X1
WD repeat and HMG-box DNA-binding protein 1 isoform X2
acetylcholine receptor subunit alpha-type acr-16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein U-like protein 1, 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 16 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein U-like protein 1, 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 50 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein U-like protein 1 isoform X2
heterogeneous nuclear ribonucleoprotein U-like protein 1 isoform X1
dynein regulatory complex protein 8-like
delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase, mitochondrial, transcript variant X1
delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase, mitochondrial, transcript variant X2
delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase, mitochondrial isoform X1
delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase, mitochondrial isoform X2
UV radiation resistance-associated gene protein, transcript variant X3
UV radiation resistance-associated gene protein, transcript variant X2
UV radiation resistance-associated gene protein, transcript variant X1
UV radiation resistance-associated gene protein, transcript variant X4
UV radiation resistance-associated gene protein isoform X2
UV radiation resistance-associated gene protein isoform X1
UV radiation resistance-associated gene protein isoform X3
uncharacterized LOC124415019, transcript variant X1
uncharacterized LOC124415019, transcript variant X3
uncharacterized LOC124415019, transcript variant X2
mitochondrial import inner membrane translocase subunit Tim10, transcript variant X1
mitochondrial import inner membrane translocase subunit Tim10, transcript variant X2
mitochondrial import inner membrane translocase subunit Tim10
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 20 samples with support for all annotated introns
E3 ubiquitin-protein ligase Nedd-4, transcript variant X1
E3 ubiquitin-protein ligase Nedd-4, transcript variant X3
E3 ubiquitin-protein ligase Nedd-4 isoform X1
E3 ubiquitin-protein ligase NEDD4 isoform X3
E3 ubiquitin-protein ligase Nedd-4, transcript variant X2
E3 ubiquitin-protein ligase Nedd-4, transcript variant X4
E3 ubiquitin-protein ligase Nedd-4 isoform X2
E3 ubiquitin-protein ligase Nedd-4 isoform X4
kin of IRRE-like protein 2, 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 3 samples with support for all annotated introns
kin of IRRE-like protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 155 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
signal recognition particle 9 kDa protein
band 4.1-like protein 4A, transcript variant X2
band 4.1-like protein 4A, transcript variant X4
band 4.1-like protein 4A, transcript variant X3
band 4.1-like protein 4A, transcript variant X1
thyroid receptor-interacting protein 11-like, transcript variant X1
thyroid receptor-interacting protein 11-like, transcript variant X3
thyroid receptor-interacting protein 11-like, transcript variant X2
thyroid receptor-interacting protein 11-like isoform X1
thyroid receptor-interacting protein 11-like isoform X3
thyroid receptor-interacting protein 11-like isoform X2
thyroid receptor-interacting protein 11-like, transcript variant X4
thyroid receptor-interacting protein 11-like isoform X4
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X7
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X3
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X9
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X4
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X6
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X10
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X5
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X8
mitogen-activated protein kinase kinase kinase kinase 5, transcript variant X11
mitogen-activated protein kinase kinase kinase kinase 5 isoform X1
mitogen-activated protein kinase kinase kinase kinase 5 isoform X7
mitogen-activated protein kinase kinase kinase kinase 5 isoform X3
mitogen-activated protein kinase kinase kinase kinase 3 isoform X9
mitogen-activated protein kinase kinase kinase kinase 5 isoform X2
mitogen-activated protein kinase kinase kinase kinase 5 isoform X4
mitogen-activated protein kinase kinase kinase kinase 5 isoform X6
mitogen-activated protein kinase kinase kinase kinase 5 isoform X10
mitogen-activated protein kinase kinase kinase kinase 5 isoform X5
mitogen-activated protein kinase kinase kinase kinase 5 isoform X8
mitogen-activated protein kinase kinase kinase kinase 3 isoform X11
ryanodine receptor, transcript variant X14
ryanodine receptor, transcript variant X10
ryanodine receptor, transcript variant X6
ryanodine receptor, transcript variant X17
ryanodine receptor, transcript variant X1
ryanodine receptor, transcript variant X2
ryanodine receptor, transcript variant X3
ryanodine receptor, transcript variant X5
ryanodine receptor, transcript variant X15
ryanodine receptor, transcript variant X4
ryanodine receptor, transcript variant X7
ryanodine receptor, transcript variant X9
ryanodine receptor, transcript variant X18
ryanodine receptor, transcript variant X13
ryanodine receptor, transcript variant X11
ryanodine receptor, transcript variant X16
ryanodine receptor, transcript variant X12
ryanodine receptor, transcript variant X8
uncharacterized LOC124414720, transcript variant X2
uncharacterized LOC124414720, transcript variant X1
uncharacterized protein LOC124414720 isoform X2
uncharacterized protein LOC124414720 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124415074, 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 23 samples with support for all annotated introns
uncharacterized protein LOC124415074 isoform X1
uncharacterized LOC124415074, 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 45 samples with support for all annotated introns
uncharacterized protein LOC124415074 isoform X2
arp2/3 complex-activating protein rickA-like
acyl-CoA synthetase short-chain family member 3, mitochondrial, transcript variant X2
acyl-CoA synthetase short-chain family member 3, mitochondrial, transcript variant X1
acyl-CoA synthetase short-chain family member 3, mitochondrial isoform X2
acyl-CoA synthetase short-chain family member 3, mitochondrial isoform X1
uncharacterized LOC124415097, transcript variant X2
uncharacterized LOC124415097, 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 17 samples with support for all annotated introns
uncharacterized protein LOC124415097 isoform X3
uncharacterized protein LOC124415097 isoform X2
uncharacterized LOC124415097, transcript variant X1
uncharacterized protein LOC124415097 isoform X1
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized protein CG43427, transcript variant X1
uncharacterized protein CG43427, transcript variant X4
uncharacterized protein CG43427, transcript variant X3
uncharacterized protein CG43427, transcript variant X2
uncharacterized protein CG43427 isoform X1
photoreceptor-specific nuclear receptor-like, transcript variant X2
photoreceptor-specific nuclear receptor-like, transcript variant X1
photoreceptor-specific nuclear receptor-like isoform X2
photoreceptor-specific nuclear receptor-like isoform X1
alkaline ceramidase, transcript variant X1
alkaline ceramidase, transcript variant X2
electron transfer flavoprotein subunit alpha, mitochondrial
uncharacterized LOC124414614, transcript variant X2
uncharacterized LOC124414614, transcript variant X3
uncharacterized LOC124414614, transcript variant X1
uncharacterized LOC124414608, transcript variant X1
uncharacterized protein LOC124414608 isoform X1
uncharacterized LOC124414608, transcript variant X2
uncharacterized protein LOC124414608 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 45 samples with support for all annotated introns
cytosolic carboxypeptidase 1-like, transcript variant X2
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 X3
cytosolic carboxypeptidase 1-like, transcript variant X4
cytosolic carboxypeptidase 1-like isoform X4
uncharacterized LOC124414609, transcript variant X1
uncharacterized LOC124414609, transcript variant X2
uncharacterized protein LOC124414609 isoform X1
uncharacterized protein LOC124414609 isoform X2
uncharacterized LOC124414609, transcript variant X3
uncharacterized protein LOC124414609 isoform X3
mitochondrial uncoupling protein 2-like, transcript variant X2
mitochondrial uncoupling protein 2-like, transcript variant X1
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ARL14 effector protein-like, transcript variant X2
ARL14 effector protein-like, transcript variant X1
AT-rich interactive domain-containing protein 3C, transcript variant X1
AT-rich interactive domain-containing protein 3C, transcript variant X3
AT-rich interactive domain-containing protein 3C, transcript variant X2
AT-rich interactive domain-containing protein 3C, transcript variant X4
AT-rich interactive domain-containing protein 3C, transcript variant X5
AT-rich interactive domain-containing protein 3C isoform X4
AT-rich interactive domain-containing protein 3C isoform X5
uncharacterized LOC124414712, transcript variant X1
uncharacterized LOC124414712, transcript variant X2
uncharacterized protein LOC124414712 isoform X1
uncharacterized protein LOC124414712 isoform X2
uncharacterized LOC124414712, transcript variant X3
uncharacterized protein LOC124414712 isoform X3
serine/arginine repetitive matrix protein 2-like, transcript variant X2
serine/arginine repetitive matrix protein 2-like, transcript variant X1
serine/arginine repetitive matrix protein 2-like isoform X2
serine/arginine repetitive matrix protein 2-like isoform X1