Vespa crabro chromosome 14, iyVesCrab1.2, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Hymenoptera; Apocrita; Aculeata; Vespoidea; Vespidae; Vespinae; Vespa.
REFSEQ INFORMATION: The reference sequence is identical to\nOU342413.1.\nAssembly name: iyVesCrab1.2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/02/09. The original whole-genome shotgun project has the\naccession CAJUUB000000000.2.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Vespa crabro Annotation Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
cytochrome P450 4C1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytochrome P450 4C1-like, transcript variant X2
inhibitor of nuclear factor kappa-B kinase subunit alpha-like, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
inhibitor of nuclear factor kappa-B kinase subunit alpha-like, transcript variant X1
inhibitor of nuclear factor kappa-B kinase subunit alpha-like, transcript variant X3
inhibitor of nuclear factor kappa-B kinase subunit alpha-like isoform X1
inhibitor of nuclear factor kappa-B kinase subunit alpha-like isoform X2
inhibitor of nuclear factor kappa-B kinase subunit alpha-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein dissatisfaction-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
protein dissatisfaction-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 1 sample with support for all annotated introns
protein dissatisfaction-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein dissatisfaction-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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
1-phosphatidylinositol 3-phosphate 5-kinase
UBA-like domain-containing protein 2, transcript variant X2
UBA-like domain-containing protein 2 isoform X2
UBA-like domain-containing protein 2, transcript variant X1
uncharacterized protein LOC124429214 isoform X1
regulator of MON1-CCZ1 complex, transcript variant X1
regulator of MON1-CCZ1 complex, transcript variant X2
regulator of MON1-CCZ1 complex isoform X1
regulator of MON1-CCZ1 complex isoform X2
single-minded homolog 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
single-minded homolog 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
single-minded homolog 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
single-minded homolog 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
single-minded homolog 2, transcript variant X7
single-minded homolog 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
single-minded homolog 2, transcript variant X9
single-minded homolog 2, transcript variant X1
single-minded homolog 2, transcript variant X2
uncharacterized LOC124429238, transcript variant X3
uncharacterized LOC124429238, transcript variant X1
uncharacterized LOC124429238, transcript variant X4
uncharacterized LOC124429238, transcript variant X2
uncharacterized protein LOC124429238 isoform X3
uncharacterized protein LOC124429238 isoform X1
uncharacterized protein LOC124429238 isoform X4
uncharacterized protein LOC124429238 isoform X2
uncharacterized LOC124429232, transcript variant X2
uncharacterized LOC124429232, transcript variant X1
uncharacterized protein LOC124429232 isoform X1
uncharacterized protein LOC124429232 isoform X2
U3 small nucleolar ribonucleoprotein protein IMP3
sodium-coupled neutral amino acid transporter 9-like, transcript variant X2
sodium-coupled neutral amino acid transporter 9-like, transcript variant X1
sodium-coupled neutral amino acid transporter 9-like isoform X1
sodium-coupled neutral amino acid transporter 9-like, transcript variant X3
sodium-coupled neutral amino acid transporter 9-like isoform X2
ATP synthase subunit C lysine N-methyltransferase, 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 16 samples with support for all annotated introns
ATP synthase subunit C lysine N-methyltransferase, transcript variant X2
ATP synthase subunit C lysine N-methyltransferase
EF-hand calcium-binding domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC124429158, 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 8 samples with support for all annotated introns
uncharacterized LOC124429158, 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 1 sample with support for all annotated introns
uncharacterized LOC124429158, transcript variant X2
uncharacterized protein LOC124429158 isoform X1
uncharacterized protein LOC124429158 isoform X3
uncharacterized protein LOC124429158 isoform X2
glycine-rich cell wall structural protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124428998, transcript variant X1
uncharacterized LOC124428998, transcript variant X2
uncharacterized transmembrane protein DDB_G0289901-like isoform X4
uncharacterized transmembrane protein DDB_G0289901-like 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 17 samples with support for all annotated introns
uncharacterized transmembrane protein DDB_G0289901-like isoform X3
glutaminase kidney isoform, mitochondrial, transcript variant X5
glutaminase kidney isoform, mitochondrial, transcript variant X2
glutaminase kidney isoform, mitochondrial, transcript variant X1
glutaminase kidney isoform, mitochondrial, transcript variant X4
glutaminase kidney isoform, mitochondrial, transcript variant X7
glutaminase kidney isoform, mitochondrial, transcript variant X8
glutaminase kidney isoform, mitochondrial, transcript variant X10
glutaminase kidney isoform, mitochondrial, transcript variant X9
glutaminase kidney isoform, mitochondrial, transcript variant X3
glutaminase kidney isoform, mitochondrial, transcript variant X6
glutaminase kidney isoform, mitochondrial isoform X5
glutaminase liver isoform, mitochondrial isoform X2
glutaminase kidney isoform, mitochondrial isoform X4
glutaminase liver isoform, mitochondrial isoform X1
glutaminase kidney isoform, mitochondrial isoform X8
glutaminase kidney isoform, mitochondrial isoform X7
glutaminase kidney isoform, mitochondrial isoform X10
glutaminase kidney isoform, mitochondrial isoform X9
glutaminase kidney isoform, mitochondrial isoform X6
glutaminase liver isoform, mitochondrial isoform X3
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, 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 16 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, 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 11 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized protein LOC124428951 isoform X1
uncharacterized protein LOC124428951 isoform X2
uncharacterized protein LOC124428951 isoform X3
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, transcript variant X6
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 14 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-1-interacting protein isoform X5
sodium/potassium-transporting ATPase subunit beta-1-interacting protein isoform X6
sodium/potassium-transporting ATPase subunit beta-1-interacting protein, transcript variant X4
sodium/potassium-transporting ATPase subunit beta-1-interacting protein isoform X4
OVARIAN TUMOR DOMAIN-containing deubiquitinating enzyme 7-like
short-chain dehydrogenase/reductase family 16C member 6-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 9 samples with support for all annotated introns
short-chain dehydrogenase/reductase family 16C member 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
short-chain dehydrogenase/reductase family 16C member 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phospholipid-transporting ATPase ABCA3-like
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
phospholipid-transporting ATPase ABCA3-like, transcript variant X3
phospholipid-transporting ATPase ABCA3-like, transcript variant X2
phospholipid-transporting ATPase ABCA3-like, transcript variant X5
phospholipid-transporting ATPase ABCA3-like isoform X2
phospholipid-transporting ATPase ABCA3-like, transcript variant X1
phospholipid-transporting ATPase ABCA3-like, transcript variant X6
phospholipid-transporting ATPase ABCA3-like, transcript variant X4
phospholipid-transporting ATPase ABCA3-like, transcript variant X8
ABC transporter A family member 1-like isoform X1
ATP-binding cassette sub-family A member 17-like isoform X6
phospholipid-transporting ATPase ABCA3-like isoform X4
ABC transporter A family member 1-like isoform X8
phospholipid-transporting ATPase ABCA3-like isoform X3
phospholipid-transporting ATPase ABCA3-like, transcript variant X7
phospholipid-transporting ATPase ABCA3-like isoform X5
ATP-binding cassette sub-family A member 17-like isoform X7
myb-like protein X, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myb-like protein X, transcript variant X3
myb-like protein X, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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 5 samples with support for all annotated introns
TBC1 domain family member 13, transcript variant X1
TBC1 domain family member 13, transcript variant X2
LIM/homeobox protein Awh-like, transcript variant X2
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
LIM/homeobox protein Awh-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LIM/homeobox protein Awh-like, transcript variant X3
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 6 samples with support for all annotated introns
LIM/homeobox protein Awh-like isoform X1
LIM/homeobox protein Awh-like isoform 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 3 samples with support for all annotated introns
putative uncharacterized protein DDB_G0282133
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
equilibrative nucleoside transporter 4, transcript variant X2
equilibrative nucleoside transporter 4, transcript variant X3
equilibrative nucleoside transporter 4, transcript variant X1
serine/threonine-protein kinase dyf-5, transcript variant X4
serine/threonine-protein kinase dyf-5, transcript variant X3
serine/threonine-protein kinase dyf-5, transcript variant X2
serine/threonine-protein kinase dyf-5 isoform X4
serine/threonine-protein kinase dyf-5 isoform X3
serine/threonine-protein kinase dyf-5 isoform X2
serine/threonine-protein kinase dyf-5, 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 15 samples with support for all annotated introns
serine/threonine-protein kinase ICK isoform X1
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 3-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 1 sample with support for all annotated introns
COP9 signalosome complex subunit 3, transcript variant X1
COP9 signalosome complex subunit 3, transcript variant X2
COP9 signalosome complex subunit 3 isoform X1
COP9 signalosome complex subunit 3 isoform X2
active regulator of SIRT1-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 15 samples with support for all annotated introns
active regulator of SIRT1-like, transcript variant X1
piggyBac transposable element-derived protein 4-like
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
17-beta-hydroxysteroid dehydrogenase 13-like
unconventional myosin-Va, 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 2 samples with support for all annotated introns
unconventional myosin-Va, 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 11 samples with support for all annotated introns
unconventional myosin-Va, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
unconventional myosin-Va, transcript variant X1
unconventional myosin-Va, transcript variant X7
unconventional myosin-Va, 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
unconventional myosin-Va, transcript variant X5
unconventional myosin-Va, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124428948, transcript variant X2
uncharacterized LOC124428948, transcript variant X1
purine nucleoside phosphorylase-like, transcript variant X6
purine nucleoside phosphorylase-like, transcript variant X5
purine nucleoside phosphorylase-like, transcript variant X2
purine nucleoside phosphorylase-like, transcript variant X4
purine nucleoside phosphorylase-like, transcript variant X1
purine nucleoside phosphorylase-like isoform X2
purine nucleoside phosphorylase-like isoform X1
purine nucleoside phosphorylase-like isoform X6
purine nucleoside phosphorylase-like isoform X5
purine nucleoside phosphorylase-like isoform X4
purine nucleoside phosphorylase-like, transcript variant X3
purine nucleoside phosphorylase-like isoform X3
phosducin-like protein, transcript variant X4
phosducin-like protein, transcript variant X2
phosducin-like protein, transcript variant X1
phosducin-like protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
geranylgeranyl transferase type-2 subunit alpha
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
receptor-type guanylate cyclase daf-11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
receptor-type guanylate cyclase daf-11, transcript variant X9
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
receptor-type guanylate cyclase daf-11, transcript variant X6
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 13 samples with support for all annotated introns
receptor-type guanylate cyclase daf-11, transcript variant X2
receptor-type guanylate cyclase daf-11, transcript variant X3
receptor-type guanylate cyclase daf-11, transcript variant X4
receptor-type guanylate cyclase daf-11, transcript variant X7
receptor-type guanylate cyclase daf-11, transcript variant X8
receptor-type guanylate cyclase daf-11, transcript variant X5
receptor-type guanylate cyclase daf-11 isoform X1
receptor-type guanylate cyclase daf-11 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
complement component 1 Q subcomponent-binding protein, mitochondrial
zinc transporter ZIP13 homolog, transcript variant X1
zinc transporter ZIP13 homolog, transcript variant X2
F-box/LRR-repeat protein 7, transcript variant X8
F-box/LRR-repeat protein 7, transcript variant X9
F-box/LRR-repeat protein 7, transcript variant X5
F-box/LRR-repeat protein 7, transcript variant X1
F-box/LRR-repeat protein 7, transcript variant X2
F-box/LRR-repeat protein 7, transcript variant X3
F-box/LRR-repeat protein 7, transcript variant X4
F-box/LRR-repeat protein 7, transcript variant X10
F-box/LRR-repeat protein 7, transcript variant X6
F-box/LRR-repeat protein 7, transcript variant X7
protein Skeletor, isoforms B/C, transcript variant X4
protein Skeletor, isoforms B/C, transcript variant X13
protein Skeletor, isoforms B/C, transcript variant X5
protein Skeletor, isoforms B/C, transcript variant X2
protein Skeletor, isoforms B/C, transcript variant X11
protein Skeletor, isoforms B/C, transcript variant X12
protein Skeletor, isoforms B/C, transcript variant X7
protein Skeletor, isoforms B/C, transcript variant X6
protein Skeletor, isoforms B/C, transcript variant X8
protein Skeletor, isoforms B/C, transcript variant X3
protein Skeletor, isoforms B/C, transcript variant X10
protein Skeletor, isoforms B/C, transcript variant X9
protein Skeletor, isoforms B/C, transcript variant X1
protein Skeletor, isoforms B/C, transcript variant X14
protein Skeletor, isoforms B/C isoform X1
protein Skeletor, isoforms B/C isoform 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 17 samples with support for all annotated introns
replication protein A 70 kDa DNA-binding subunit
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
inner membrane metabolite transport protein YgcS-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: inner membrane metabolite transport protein YgcS-like
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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
glutathione S-transferase D1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutathione S-transferase D1-like isoform X2
glutathione S-transferase D1-like, transcript variant X5
glutathione S-transferase D1-like isoform X3
glutathione S-transferase D1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutathione S-transferase D1-like, transcript variant X2
glutathione S-transferase D1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
glutathione S-transferase D1-like isoform X1
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X12
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X5
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X4
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X6
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X7
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X8
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X10
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X3
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X9
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X1
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X2
acid sphingomyelinase-like phosphodiesterase 3b isoform X1
acid sphingomyelinase-like phosphodiesterase 3b isoform X2
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X11
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X13
acid sphingomyelinase-like phosphodiesterase 3b isoform X3
acid sphingomyelinase-like phosphodiesterase 3b isoform X4
sodium-dependent proline transporter-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium-dependent proline transporter-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium-dependent proline transporter-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sodium-dependent proline transporter-like isoform X2
sodium- and chloride-dependent glycine transporter 1-like isoform X3
sodium-dependent proline transporter-like isoform X1
trafficking protein particle complex subunit 1
E3 ubiquitin-protein ligase RNF19A-like, transcript variant X2
E3 ubiquitin-protein ligase RNF19A-like, transcript variant X3
E3 ubiquitin-protein ligase RNF19A-like, transcript variant X1
E3 ubiquitin-protein ligase RNF19A-like isoform X2
E3 ubiquitin-protein ligase RNF19A-like isoform X1
uncharacterized LOC124429006, transcript variant X1
uncharacterized LOC124429006, transcript variant X3
uncharacterized LOC124429006, transcript variant X2
synaptic functional regulator FMR1, transcript variant X1
synaptic functional regulator FMR1, transcript variant X5
synaptic functional regulator FMR1, transcript variant X3
synaptic functional regulator FMR1, transcript variant X2
synaptic functional regulator FMR1, transcript variant X4
synaptic functional regulator FMR1 isoform X5
synaptic functional regulator FMR1 isoform X3
synaptic functional regulator FMR1 isoform X2
synaptic functional regulator FMR1 isoform X4
synaptic functional regulator FMR1 isoform X1
synaptic functional regulator FMR1, transcript variant X6
synaptic functional regulator FMR1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
synaptic functional regulator FMR1 isoform X7
synaptic functional regulator FMR1 isoform X6
WD repeat-containing protein 44, transcript variant X1
WD repeat-containing protein 44, transcript variant X3
WD repeat-containing protein 44, transcript variant X2
WD repeat-containing protein 44, transcript variant X4
WD repeat-containing protein 44 isoform X1
WD repeat-containing protein 44 isoform X3
WD repeat-containing protein 44 isoform X2
WD repeat-containing protein 44 isoform X4
uncharacterized LOC124429093, 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 8 samples with support for all annotated introns
uncharacterized LOC124429093, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC124429093, transcript variant X5
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 2 samples with support for all annotated introns
uncharacterized LOC124429093, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124429093, transcript variant X3
uncharacterized LOC124429093, transcript variant X4
uncharacterized LOC124429090, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124429090, 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 6 samples with support for all annotated introns
uncharacterized LOC124429090, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC124429090, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124429090, transcript variant X2
uncharacterized protein LOC124429090 isoform X2
uncharacterized protein LOC124429090 isoform X1
suppressor of lurcher protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 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
suppressor of lurcher protein 1, 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 13 samples with support for all annotated introns
NADP-dependent malic enzyme-like, transcript variant X2
NADP-dependent malic enzyme-like, transcript variant X1
NADP-dependent malic enzyme-like isoform X2
NADP-dependent malic enzyme-like isoform X1
tubby-related protein 4, transcript variant X6
tubby-related protein 4, transcript variant X5
tubby-related protein 4, transcript variant X1
tubby-related protein 4, transcript variant X2
tubby-related protein 4, transcript variant X4
tubby-related protein 4, transcript variant X3
sphingosine-1-phosphate lyase, transcript variant X1
sphingosine-1-phosphate lyase, transcript variant X2
sphingosine-1-phosphate lyase, transcript variant X3
sphingosine-1-phosphate lyase isoform X1
sphingosine-1-phosphate lyase isoform X2
uncharacterized LOC124428987, transcript variant X2
uncharacterized LOC124428987, transcript variant X1
tachykinin-like peptides receptor 99D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
tachykinin-like peptides receptor 99D, 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 12 samples with support for all annotated introns
tachykinin-like peptides receptor 99D, transcript variant X3
tachykinin-like peptides receptor 99D isoform X2
tachykinin-like peptides receptor 99D isoform X1
peptide deformylase, mitochondrial-like, 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 12 samples with support for all annotated introns
peptide deformylase, mitochondrial-like, transcript variant X1
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial-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 18 samples with support for all annotated introns
uncharacterized LOC124429097, transcript variant X3
uncharacterized LOC124429097, transcript variant X2
uncharacterized LOC124429097, transcript variant X1
uncharacterized LOC124429097, transcript variant X4
uncharacterized LOC124429097, transcript variant X5
uncharacterized LOC124429097, transcript variant X6
uncharacterized protein LOC124429097 isoform X1
uncharacterized protein LOC124429097 isoform X3
uncharacterized protein LOC124429097 isoform X2
uncharacterized protein LOC124429097 isoform X4
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein disulfide-isomerase TMX3, transcript variant X2
protein disulfide-isomerase TMX3, transcript variant X1
protein disulfide-isomerase TMX3 isoform X2
protein disulfide-isomerase TMX3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124428955, transcript variant X1
uncharacterized LOC124428955, transcript variant X2
uncharacterized protein LOC124428955 isoform X1
uncharacterized protein LOC124428955 isoform X2
protein disulfide-isomerase, transcript variant X3
protein disulfide-isomerase, transcript variant X2
protein disulfide-isomerase, transcript variant X4
protein disulfide-isomerase, transcript variant X1
methyltransferase-like protein 22, transcript variant X4
methyltransferase-like protein 22, transcript variant X2
methyltransferase-like protein 22, transcript variant X3
methyltransferase-like protein 22, transcript variant X1
methyltransferase-like protein 22 isoform X1
methyltransferase-like protein 22, transcript variant X5
methyltransferase-like protein 22 isoform X2
methyltransferase-like protein 22 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
polycomb protein suz12-B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
polycomb protein suz12-B, transcript variant X1
ubiquitin domain-containing protein UBFD1-like, transcript variant X4
ubiquitin domain-containing protein UBFD1-like isoform X3
ubiquitin domain-containing protein UBFD1-like, transcript variant X3
ubiquitin domain-containing protein UBFD1-like isoform X2
ubiquitin domain-containing protein UBFD1-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 10 samples with support for all annotated introns
ubiquitin domain-containing protein UBFD1-like, transcript variant X1
ubiquitin domain-containing protein UBFD1-like, transcript variant X5
ubiquitin domain-containing protein UBFD1-like isoform X1
ubiquitin domain-containing protein UBFD1-like isoform 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 16 samples with support for all annotated introns
WW domain-binding protein 2, transcript variant X2
WW domain-binding protein 2, transcript variant X1
calcium-dependent secretion activator, transcript variant X1
calcium-dependent secretion activator, transcript variant X2
calcium-dependent secretion activator isoform X1
calcium-dependent secretion activator isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC124429268, transcript variant X2
uncharacterized LOC124429268, transcript variant X3
uncharacterized LOC124429268, transcript variant X4
uncharacterized LOC124429268, transcript variant X1
uncharacterized protein LOC124429268 isoform X2
uncharacterized protein LOC124429268 isoform X1
vacuolar ATPase assembly integral membrane protein VMA21 homolog
97 kDa heat shock protein, transcript variant X1
97 kDa heat shock protein, transcript variant X2
caseinolytic peptidase B protein homolog
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
vacuolar protein-sorting-associated protein 36, transcript variant X1
vacuolar protein-sorting-associated protein 36, transcript variant X2
vacuolar protein-sorting-associated protein 36
uncharacterized LOC124429172, transcript variant X3
uncharacterized LOC124429172, transcript variant X4
uncharacterized LOC124429172, transcript variant X2
uncharacterized LOC124429172, transcript variant X1
uncharacterized LOC124429001, transcript variant X1
uncharacterized LOC124429001, transcript variant X2
uncharacterized LOC124429000, transcript variant X1
uncharacterized LOC124429000, transcript variant X2
LIM domain kinase 1, transcript variant X1
LIM domain kinase 1, transcript variant X2
optomotor-blind protein, transcript variant X3
optomotor-blind protein, transcript variant X1
optomotor-blind protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
optomotor-blind protein, transcript variant X2
optomotor-blind protein, transcript variant X6
optomotor-blind protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Fanconi anemia group J protein homolog, transcript variant X1
Fanconi anemia group J protein homolog, transcript variant X3
Fanconi anemia group J protein homolog, transcript variant X2
Fanconi anemia group J protein homolog isoform X1
Fanconi anemia group J protein homolog isoform X2
Fanconi anemia group J protein homolog isoform X3
coiled-coil domain-containing protein 86
phospholipase A2 isozymes PA3A/PA3B/PA5, transcript variant X1
phospholipase A2 isozymes PA3A/PA3B/PA5, transcript variant X3
phospholipase A2 isozymes PA3A/PA3B/PA5, transcript variant X2
phospholipase A2 isozymes PA3A/PA3B/PA5 isoform X2
uncharacterized protein LOC124429083 isoform X1
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 15 samples with support for all annotated introns
arginine/serine-rich coiled-coil protein 2, transcript variant X1
arginine/serine-rich coiled-coil protein 2, transcript variant X4
arginine/serine-rich coiled-coil protein 2, transcript variant X3
arginine/serine-rich coiled-coil protein 2, transcript variant X2
arginine/serine-rich coiled-coil protein 2 isoform X1
arginine/serine-rich coiled-coil protein 2 isoform X2
arginine/serine-rich coiled-coil protein 2 isoform X3
nuclear transcription factor Y subunit alpha, transcript variant X2
nuclear transcription factor Y subunit alpha, transcript variant X1
nuclear transcription factor Y subunit alpha, transcript variant X3
nuclear transcription factor Y subunit alpha
U8-agatoxin-Ao1a-like, transcript variant X2
U8-agatoxin-Ao1a-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 5 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 12 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; 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 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC124428994
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
heme transporter hrg1-A-like, transcript variant X1
heme transporter hrg1-A-like, transcript variant X5
uncharacterized protein LOC124428992 isoform X3
uncharacterized protein LOC124428992 isoform X1
heme transporter hrg1-A-like, transcript variant X3
heme transporter hrg1-A-like, transcript variant X4
heme transporter hrg1-A-like, transcript variant X2
peroxisomal membrane protein 11B, transcript variant X2
peroxisomal membrane protein 11B, transcript variant X1
ADP-ribosylation factor-like protein 6-interacting protein 1
DNA-directed RNA polymerase III subunit RPC6, transcript variant X2
DNA-directed RNA polymerase III subunit RPC6, transcript variant X1
probable DNA-directed RNA polymerase III subunit RPC6 isoform X1
DNA-directed RNA polymerase III subunit RPC6 isoform X2
dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial, transcript variant X2
dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial, transcript variant X1
dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial
trafficking protein particle complex subunit 8
tudor domain-containing protein 7-like, transcript variant X1
tudor domain-containing protein 7-like, transcript variant X5
tudor domain-containing protein 7-like, transcript variant X3
tudor domain-containing protein 7-like, transcript variant X2
tudor domain-containing protein 7-like, transcript variant X4
adenylyl cyclase 78C-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
adenylyl cyclase 78C-like, transcript variant X1
adenylyl cyclase 78C-like, transcript variant X3
adenylyl cyclase 78C-like, transcript variant X2
adenylyl cyclase 78C-like, transcript variant X4
histone demethylase UTY, transcript variant X3
histone demethylase UTY, transcript variant X1
histone demethylase UTY, transcript variant X2
histone demethylase UTY, transcript variant X5
histone demethylase UTY, transcript variant X4
histone demethylase UTY, transcript variant X6
FUN14 domain-containing protein 1A, transcript variant X3
FUN14 domain-containing protein 1A, transcript variant X4
FUN14 domain-containing protein 1A, transcript variant X5
FUN14 domain-containing protein 1A, transcript variant X1
uncharacterized protein LOC124428963 isoform X1
FUN14 domain-containing protein 1A isoform X4
FUN14 domain-containing protein 1A, transcript variant X2
FUN14 domain-containing protein 2 isoform X2
FUN14 domain-containing protein 2 isoform X3
metallo-beta-lactamase domain-containing protein 1, transcript variant X2
metallo-beta-lactamase domain-containing protein 1, transcript variant X1
metallo-beta-lactamase domain-containing protein 1 isoform X1
metallo-beta-lactamase domain-containing protein 1 isoform X2
sodium/hydrogen exchanger 6, transcript variant X5
sodium/hydrogen exchanger 6, transcript variant X8
sodium/hydrogen exchanger 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
sodium/hydrogen exchanger 6, transcript variant X9
sodium/hydrogen exchanger 6, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
sodium/hydrogen exchanger 6, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
sodium/hydrogen exchanger 6, transcript variant X3
sodium/hydrogen exchanger 6, transcript variant X2
sodium/hydrogen exchanger 6, transcript variant X4
conserved oligomeric Golgi complex subunit 3
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 18 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 1, transcript variant X3
conserved oligomeric Golgi complex subunit 1, 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 11 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 1, transcript variant X2
conserved oligomeric Golgi complex subunit 1 isoform X1
conserved oligomeric Golgi complex subunit 1 isoform X2
ras-related protein Rab-32, transcript variant X5
ras-related protein Rab-32, transcript variant X4
ras-related protein Rab-32, transcript variant X1
ras-related protein Rab-32, transcript variant X2
ras-related protein Rab-32, transcript variant X3
uncharacterized protein LOC124429024 isoform X1
uncharacterized protein LOC124429024 isoform X2
uncharacterized protein LOC124429024 isoform X3
ras-related protein Rab-32, transcript variant X6
uncharacterized LOC124429239, transcript variant X1
uncharacterized LOC124429239, transcript variant X8
uncharacterized LOC124429239, transcript variant X2
uncharacterized LOC124429239, transcript variant X4
uncharacterized LOC124429239, transcript variant X5
uncharacterized LOC124429239, transcript variant X3
uncharacterized LOC124429239, transcript variant X6
uncharacterized LOC124429239, transcript variant X10
uncharacterized LOC124429239, transcript variant X12
uncharacterized LOC124429239, transcript variant X7
uncharacterized LOC124429239, transcript variant X9
uncharacterized LOC124429239, transcript variant X11
uncharacterized protein LOC124429239 isoform X1
uncharacterized protein LOC124429239 isoform X8
uncharacterized protein LOC124429239 isoform X6
uncharacterized protein LOC124429239 isoform X10
uncharacterized protein LOC124429239 isoform X12
uncharacterized protein LOC124429239 isoform X7
uncharacterized protein LOC124429239 isoform X2
uncharacterized protein LOC124429239 isoform X9
uncharacterized protein LOC124429239 isoform X11
uncharacterized protein LOC124429239 isoform X4
uncharacterized protein LOC124429239 isoform X5
uncharacterized protein LOC124429239 isoform X3
uncharacterized LOC124429239, transcript variant X13
uncharacterized LOC124429239, transcript variant X14
uncharacterized protein LOC124429239 isoform X13
protein scarlet-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein scarlet-like, transcript variant X2
probable peroxisomal acyl-coenzyme A oxidase 1
translation initiation factor eIF-2B subunit delta, transcript variant X2
translation initiation factor eIF-2B subunit delta, transcript variant X5
translation initiation factor eIF-2B subunit delta, transcript variant X4
translation initiation factor eIF-2B subunit delta, transcript variant X3
translation initiation factor eIF-2B subunit delta isoform X2
translation initiation factor eIF-2B subunit delta, transcript variant X1
translation initiation factor eIF-2B subunit delta isoform X1
translation initiation factor eIF-2B subunit delta isoform X3
transcription termination factor 5, mitochondrial, 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 14 samples with support for all annotated introns
transcription termination factor 5, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
transcription termination factor 5, mitochondrial isoform X1
uncharacterized protein LOC124428976 isoform X2
homeobox protein orthopedia B, transcript variant X3
homeobox protein orthopedia B, transcript variant X2
homeobox protein orthopedia B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC124429109, transcript variant X1
uncharacterized LOC124429109, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
phospholipid scramblase 1, transcript variant X4
phospholipid scramblase 1, transcript variant X5
phospholipid scramblase 1, transcript variant X6
phospholipid scramblase 1, transcript variant X2
phospholipid scramblase 1, transcript variant X1
phospholipid scramblase 1, transcript variant X3
1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase
ribonucleoside-diphosphate reductase subunit M2 B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
ribonucleoside-diphosphate reductase subunit M2 B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
ribonucleoside-diphosphate reductase subunit M2 B isoform X1
ribonucleoside-diphosphate reductase subunit M2 B isoform X2
cullin-associated NEDD8-dissociated protein 1, transcript variant X3
cullin-associated NEDD8-dissociated protein 1, transcript variant X2
cullin-associated NEDD8-dissociated protein 1, transcript variant X1
cullin-associated NEDD8-dissociated protein 1 isoform X2
cullin-associated NEDD8-dissociated protein 1 isoform 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
protein N-terminal asparagine amidohydrolase, transcript variant X4
protein N-terminal asparagine amidohydrolase, transcript variant X3
protein N-terminal asparagine amidohydrolase, transcript variant X1
protein N-terminal asparagine amidohydrolase, transcript variant X2
protein N-terminal asparagine amidohydrolase, transcript variant X6
protein N-terminal asparagine amidohydrolase, transcript variant X5
protein N-terminal asparagine amidohydrolase
cytosolic Fe-S cluster assembly factor NUBP1 homolog, transcript variant X2
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 10 samples with support for all annotated introns
cytosolic Fe-S cluster assembly factor NUBP1 homolog isoform X2
cytosolic Fe-S cluster assembly factor NUBP1 homolog, transcript variant X1
cytosolic Fe-S cluster assembly factor NUBP1 homolog isoform X1
cytochrome c oxidase assembly protein COX11, mitochondrial
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X15
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 14 samples with support for all annotated introns
longitudinals lacking protein-like isoform X13
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X45
longitudinals lacking protein, isoforms F/I/K/T-like isoform X43
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X24
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 15 samples with support for all annotated introns
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X44
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X19
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X34
longitudinals lacking protein, isoforms N/O/W/X/Y-like isoform X32
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X31
longitudinals lacking protein, isoforms A/B/D/L-like isoform X29
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X6
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X26
longitudinals lacking protein, isoforms A/B/D/L-like isoform X24
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
longitudinals lacking protein-like isoform X3
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X30
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X38
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X33
longitudinals lacking protein, isoforms A/B/D/L-like isoform X31
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X16
longitudinals lacking protein, isoforms F/I/K/T-like isoform X14
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X11
longitudinals lacking protein, isoforms N/O/W/X/Y-like isoform X9
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X36
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X4
longitudinals lacking protein, isoforms F/I/K/T-like isoform X2
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X48
longitudinals lacking protein, isoforms A/B/D/L-like isoform X46
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X7
longitudinals lacking protein, isoforms A/B/D/L-like isoform X5
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X28
longitudinals lacking protein-like isoform X26
zinc finger and BTB domain-containing protein 6-like
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X1
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X32
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 16 samples with support for all annotated introns
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X18
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X2
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X3
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 4 samples with support for all annotated introns
longitudinals lacking protein-like isoform X30
longitudinals lacking protein-like isoform X16
longitudinals lacking protein, isoforms A/B/D/L-like isoform X1
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X42
longitudinals lacking protein, isoforms A/B/D/L-like isoform X40
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X37
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 8 samples with support for all annotated introns
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X25
longitudinals lacking protein, isoforms A/B/D/L-like isoform X35
longitudinals lacking protein, isoforms A/B/D/L-like isoform X23
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X39
longitudinals lacking protein, isoforms A/B/D/L-like isoform X37
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X14
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 6 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X12
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X40
longitudinals lacking protein-like isoform X38
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X46
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 4 samples with support for all annotated introns
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X43
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X21
longitudinals lacking protein, isoforms A/B/D/L-like isoform X44
longitudinals lacking protein, isoforms A/B/D/L-like isoform X41
longitudinals lacking protein, isoforms A/B/D/L-like isoform X19
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X27
longitudinals lacking protein, isoforms A/B/D/L-like isoform X25
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X47
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
longitudinals lacking protein, isoforms A/B/D/L-like isoform X45
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X49
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X17
longitudinals lacking protein, isoforms A/B/D/L-like isoform X47
longitudinals lacking protein, isoforms N/O/W/X/Y-like isoform X15
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X6
zinc finger and BTB domain-containing protein 5-like isoform X4
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X20
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 9 samples with support for all annotated introns
longitudinals lacking protein, isoforms A/B/D/L-like isoform X18
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X29
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X22
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X23
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X13
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 13 samples with support for all annotated introns
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X12
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X10
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X41
ras-interacting protein RIP3-like isoform X8
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X9
longitudinals lacking protein, isoforms F/I/K/T-like, transcript variant X35
longitudinals lacking protein, isoforms A/B/D/L-like isoform X33
longitudinals lacking protein, isoforms A/B/D/L-like isoform X7
carbonic anhydrase 7-like, transcript variant X2
uncharacterized LOC124429030, transcript variant X3
zinc finger CCCH domain-containing protein 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124429030, transcript variant X2
uncharacterized protein LOC124429030 isoform X2
uncharacterized protein LOC124429030 isoform X3
uncharacterized LOC124429030, transcript variant X1
uncharacterized protein LOC124429030 isoform X1
uncharacterized LOC124429030, transcript variant X4
uncharacterized protein LOC124429030 isoform X4
adenosine 5'-monophosphoramidase HINT3-like
mitochondrial enolase superfamily member 1-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 15 samples with support for all annotated introns
collagen alpha chain CG42342, transcript variant X7
collagen alpha chain CG42342, transcript variant X5
collagen alpha chain CG42342, transcript variant X3
collagen alpha chain CG42342, transcript variant X2
collagen alpha chain CG42342, transcript variant X4
collagen alpha chain CG42342, transcript variant X10
collagen alpha chain CG42342, transcript variant X1
collagen alpha chain CG42342, transcript variant X8
collagen alpha chain CG42342, transcript variant X6
collagen alpha chain CG42342, transcript variant X11
collagen alpha chain CG42342, transcript variant X13
collagen alpha chain CG42342, transcript variant X9
collagen alpha chain CG42342, transcript variant X16
collagen alpha chain CG42342, transcript variant X15
collagen alpha chain CG42342, transcript variant X14
collagen alpha chain CG42342, transcript variant X12
collagen alpha chain CG42342 isoform X11
collagen alpha chain CG42342 isoform X10
collagen alpha chain CG42342 isoform X13
collagen alpha chain CG42342 isoform X16
collagen alpha chain CG42342 isoform X15
collagen alpha chain CG42342 isoform X14
collagen alpha chain CG42342 isoform X12
uncharacterized LOC124429052, transcript variant X1
uncharacterized LOC124429052, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC124429052 isoform X1
uncharacterized protein LOC124429052 isoform X2
urea transporter 2-like, transcript variant X1
urea transporter 2-like, transcript variant X2
urea transporter 2-like, transcript variant X3
lateral signaling target protein 2 homolog, transcript variant X2
lateral signaling target protein 2 homolog, transcript variant X1
lateral signaling target protein 2 homolog isoform X2
lateral signaling target protein 2 homolog isoform X1
facilitated trehalose transporter Tret1-like
leucine-rich PPR motif-containing protein, mitochondrial-like, transcript variant X2
leucine-rich PPR motif-containing protein, mitochondrial-like, transcript variant X1
leucine-rich PPR motif-containing protein, mitochondrial-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 15 samples with support for all annotated introns
leucine-rich PPR motif-containing protein, mitochondrial-like isoform X2
leucine-rich PPR motif-containing protein, mitochondrial-like isoform X1
leucine-rich PPR motif-containing protein, mitochondrial-like isoform X3
ras-related protein Rap-2a, transcript variant X1
ras-related protein Rap-2a, 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 13 samples with support for all annotated introns
TBC1 domain family member 1, transcript variant X2
TBC1 domain family member 1, transcript variant X3
TBC1 domain family member 1, transcript variant X1
TBC1 domain family member 1, transcript variant X4
elongator complex protein 3, transcript variant X1
elongator complex protein 3, transcript variant X2
protein-tyrosine sulfotransferase, transcript variant X2
protein-tyrosine sulfotransferase, transcript variant X1
protein-tyrosine sulfotransferase isoform X1
protein-tyrosine sulfotransferase isoform X2
RNA exonuclease 4, transcript variant X2
RNA exonuclease 4, transcript variant X1
RNA exonuclease 4, transcript variant X3
flavin-containing monooxygenase FMO GS-OX5-like, transcript variant X1
flavin-containing monooxygenase FMO GS-OX5-like, transcript variant X2
flavin-containing monooxygenase FMO GS-OX5-like, transcript variant X4
flavin-containing monooxygenase FMO GS-OX5-like, transcript variant X3
flavin-containing monooxygenase FMO GS-OX5-like isoform X1
flavin-containing monooxygenase FMO GS-OX5-like isoform X2
GTP-binding protein SAR1, transcript variant X1
GTP-binding protein SAR1, transcript variant X2
50S ribosomal protein L1, transcript variant X2
50S ribosomal protein L1, transcript variant X1
uncharacterized protein C15orf61 homolog, transcript variant X2
uncharacterized protein C15orf61 homolog isoform X2
uncharacterized protein C15orf61 homolog, transcript variant X1
uncharacterized protein C15orf61 homolog isoform X1
tetraspanin-11-like, transcript variant X2
tetraspanin-11-like, transcript variant X1
carbonic anhydrase 7-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 2 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 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: 2 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: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
homeobox protein MSH-C-like, 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 1 sample with support for all annotated introns
homeobox protein MSH-C-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
homeobox protein engrailed-2-A-like isoform X1
uncharacterized LOC124429256, transcript variant X1
uncharacterized LOC124429256, transcript variant X2
uncharacterized protein LOC124429256 isoform X1
uncharacterized protein LOC124429256 isoform X2
disintegrin and metalloproteinase domain-containing protein 10, transcript variant X2
disintegrin and metalloproteinase domain-containing protein 10, transcript variant X1
disintegrin and metalloproteinase domain-containing protein 10, transcript variant X3
disintegrin and metalloproteinase domain-containing protein 10 isoform X1
disintegrin and metalloproteinase domain-containing protein 10 isoform X2
membrane-associated protein Hem, transcript variant X1
membrane-associated protein Hem, transcript variant X2
CUGBP Elav-like family member 4, transcript variant X6
CUGBP Elav-like family member 4, transcript variant X7
CUGBP Elav-like family member 4, transcript variant X12
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
CUGBP Elav-like family member 4, transcript variant X5
CUGBP Elav-like family member 4, transcript variant X10
CUGBP Elav-like family member 4, transcript variant X3
CUGBP Elav-like family member 4, transcript variant X8
CUGBP Elav-like family member 4, transcript variant X4
CUGBP Elav-like family member 4, transcript variant X9
CUGBP Elav-like family member 4, transcript variant X1
CUGBP Elav-like family member 4, transcript variant X11
CUGBP Elav-like family member 4, transcript variant X2
CUGBP Elav-like family member 4 isoform X1
CUGBP Elav-like family member 4 isoform X3
CUGBP Elav-like family member 4 isoform X6
CUGBP Elav-like family member 4 isoform X4
CUGBP Elav-like family member 4 isoform X7
CUGBP Elav-like family member 4 isoform X2
CUGBP Elav-like family member 4 isoform X5
CUGBP Elav-like family member 4 isoform X8
CUGBP Elav-like family member 4, transcript variant X13
CUGBP Elav-like family member 4 isoform X9
carboxypeptidase Q-like, transcript variant X4
carboxypeptidase Q-like, transcript variant X1
carboxypeptidase Q-like, transcript variant X5
carboxypeptidase Q-like, transcript variant X6
carboxypeptidase Q-like, transcript variant X3
carboxypeptidase Q-like, transcript variant X2
protein unc-80 homolog, transcript variant X4
protein unc-80 homolog, transcript variant X2
protein unc-80 homolog, transcript variant X8
protein unc-80 homolog, transcript variant X6
protein unc-80 homolog, transcript variant X7
protein unc-80 homolog, transcript variant X10
protein unc-80 homolog, transcript variant X3
protein unc-80 homolog, transcript variant X9
protein unc-80 homolog, transcript variant X5
protein unc-80 homolog, transcript variant X11
protein unc-80 homolog, transcript variant X1
protein unc-80 homolog, transcript variant X13
protein unc-80 homolog, transcript variant X12
protein unc-80 homolog, transcript variant X19
protein unc-80 homolog, transcript variant X14
protein unc-80 homolog, transcript variant X16
protein unc-80 homolog, transcript variant X15
protein unc-80 homolog, transcript variant X17
protein unc-80 homolog, transcript variant X18
uncharacterized LOC124429225, transcript variant X3
uncharacterized LOC124429225, transcript variant X1
uncharacterized LOC124429225, transcript variant X2
uncharacterized LOC124429225, transcript variant X4
uncharacterized protein LOC124429225 isoform X1
uncharacterized protein LOC124429225 isoform X2
uncharacterized protein LOC124429225 isoform X3
myosin light chain alkali, transcript variant X2
myosin light chain alkali, transcript variant X1
microtubule-associated protein 2, transcript variant X1
microtubule-associated protein 2, transcript variant X3
microtubule-associated protein 2, transcript variant X2
microtubule-associated protein 2 isoform X1
microtubule-associated protein 2 isoform X3
microtubule-associated protein 2 isoform X2
uncharacterized protein DDB_G0290587-like
cyclin-dependent kinase 2-like, transcript variant X1
cyclin-dependent kinase 2-like, transcript variant X2
cyclin-dependent kinase 2-like isoform X2
cyclin-dependent kinase 2-like isoform X1
U4/U6.U5 tri-snRNP-associated protein 1, transcript variant X1
U4/U6.U5 tri-snRNP-associated protein 1, transcript variant X2
U4/U6.U5 tri-snRNP-associated protein 1 isoform X1
U4/U6.U5 tri-snRNP-associated protein 1 isoform X2