Maniola jurtina chromosome 2, ilManJurt1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Nymphalidae; Satyrinae; Satyrini; Maniolina; Maniola.
REFSEQ INFORMATION: The reference sequence is identical to\nHG995209.1.\nAssembly name: ilManJurt1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/03/19. The original whole-genome shotgun project has the\naccession CAJOSP000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Maniola jurtina Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 3% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome cell adhesion molecule-like protein Dscam2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, 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: 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: 72% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Down syndrome cell adhesion molecule-like protein Dscam2, transcript variant X1
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X1
uncharacterized oxidoreductase SERP2049-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Down syndrome cell adhesion molecule-like protein Dscam2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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
atrial natriuretic peptide-converting enzyme
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
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: 9 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitotic spindle assembly checkpoint protein MAD2B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 98% 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: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 47% coverage of the annotated genomic feature by RNAseq alignments
protein lethal(2)essential for life-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
heat shock protein 67B1-like, transcript variant X1
heat shock protein 67B1-like, transcript variant X3
heat shock protein 67B1-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
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: 4 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: 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: 2 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
myrosinase 1-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 5 samples with support for all annotated introns
myrosinase 1-like, transcript variant 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 19 samples with support for all annotated introns
zinc transporter 2-like, transcript variant X4
zinc transporter 2-like, transcript variant X2
zinc transporter 2-like, transcript variant X1
zinc transporter 2-like, transcript variant X3
probable flavin-containing monoamine oxidase A
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: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
kinesin-like protein Klp10A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
kinesin-like protein Klp10A, 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 5 samples with support for all annotated introns
bifunctional arginine demethylase and lysyl-hydroxylase PSR
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 27 samples with support for all annotated introns
cytochrome c oxidase subunit 5A, mitochondrial
DNA-binding protein Ewg, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DNA-binding protein Ewg, 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
DNA-binding protein Ewg, 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 7 samples with support for all annotated introns
DNA-binding protein Ewg, 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 5 samples with support for all annotated introns
DNA-binding protein Ewg, transcript variant X7
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
DNA-binding protein Ewg, transcript variant X6
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
DNA-binding protein Ewg, 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 5 samples with support for all annotated introns
DNA-binding protein Ewg, transcript variant X1
DNA-binding protein Ewg, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
5-demethoxyubiquinone hydroxylase, mitochondrial, transcript variant X3
5-demethoxyubiquinone hydroxylase, mitochondrial, transcript variant X1
5-demethoxyubiquinone hydroxylase, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
5-demethoxyubiquinone hydroxylase, mitochondrial
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
scm-like with four MBT domains protein 1
translocon-associated protein subunit beta
centromere/kinetochore protein zw10 homolog
RCC1-like G exchanging factor-like protein
mediator of RNA polymerase II transcription subunit 27
neuronal acetylcholine receptor subunit alpha-7-like
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fibrous sheath CABYR-binding protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
liver carboxylesterase 1F, 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 1 sample with support for all annotated introns
liver carboxylesterase 1F, 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 6 samples with support for all annotated introns
uncharacterized LOC123877306, transcript variant X2
uncharacterized LOC123877306, transcript variant X1
uncharacterized protein LOC123877306 isoform X2
uncharacterized protein LOC123877306 isoform X1
17-beta-hydroxysteroid dehydrogenase 13-like, transcript variant X2
17-beta-hydroxysteroid dehydrogenase 13-like, transcript variant X1
17-beta-hydroxysteroid dehydrogenase 13-like isoform X2
17-beta-hydroxysteroid dehydrogenase 13-like isoform X1
oxysterol-binding protein-related protein 1, transcript variant X14
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
oxysterol-binding protein-related protein 1 isoform X8
oxysterol-binding protein-related protein 1, 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 1 sample with support for all annotated introns
oxysterol-binding protein-related protein 2 isoform X5
oxysterol-binding protein-related protein 1, transcript variant X6
oxysterol-binding protein-related protein 2 isoform X6
oxysterol-binding protein-related protein 1, transcript variant X4
oxysterol-binding protein-related protein 1, transcript variant X1
oxysterol-binding protein-related protein 2 isoform X1
oxysterol-binding protein-related protein 2 isoform X4
oxysterol-binding protein-related protein 1, transcript variant X3
oxysterol-binding protein-related protein 1, transcript variant X2
oxysterol-binding protein-related protein 2 isoform X2
oxysterol-binding protein-related protein 2 isoform X3
oxysterol-binding protein-related protein 1, 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 7 samples with support for all annotated introns
oxysterol-binding protein-related protein 1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
oxysterol-binding protein-related protein 1, transcript variant X8
oxysterol-binding protein-related protein 1, transcript variant X12
oxysterol-binding protein-related protein 1, transcript variant X10
oxysterol-binding protein-related protein 1, transcript variant X11
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
oxysterol-binding protein-related protein 1, transcript variant X13
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 7 samples with support for all annotated introns
oxysterol-binding protein-related protein 1 isoform 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 6 samples with support for all annotated introns
EF-hand calcium-binding domain-containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
EF-hand calcium-binding domain-containing 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 1 sample with support for all annotated introns
EF-hand calcium-binding domain-containing protein 1 isoform X1
EF-hand calcium-binding domain-containing protein 1 isoform X2
uncharacterized LOC123877431, transcript variant X1
uncharacterized LOC123877431, transcript variant X3
uncharacterized LOC123877431, transcript variant X2
1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase, transcript variant X1
1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase
low molecular weight phosphotyrosine protein phosphatase-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: low molecular weight phosphotyrosine protein phosphatase-like
chromatin accessibility complex 16kD protein
uncharacterized LOC123874525, transcript variant X3
uncharacterized LOC123874525, transcript variant X1
uncharacterized LOC123874525, transcript variant X2
uncharacterized LOC123874456, transcript variant X1
uncharacterized LOC123874456, transcript variant X2
uncharacterized protein LOC123874456 isoform X2
uncharacterized protein LOC123874456 isoform 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
GPI mannosyltransferase 4, transcript variant X3
GPI mannosyltransferase 4, 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 22 samples with support for all annotated introns
GPI mannosyltransferase 4, transcript variant X2
GPI mannosyltransferase 4, 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 2 samples with support for all annotated introns
histone deacetylase 6, transcript variant X1
histone deacetylase 6, transcript variant X3
histone deacetylase 6, transcript variant X4
histone deacetylase 6, transcript variant X2
histone deacetylase 6, transcript variant X5
mitochondrial intermediate peptidase, transcript variant X1
mitochondrial intermediate peptidase, transcript variant X2
mitochondrial intermediate peptidase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
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
ras-related protein Rab6, 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 8 samples with support for all annotated introns
ras-related protein Rab6, transcript variant X2
U2 snRNP-associated SURP motif-containing protein
kinesin-like protein KIF21A, 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 1 sample with support for all annotated introns
kinesin-like protein KIF21A, 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 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123870873, transcript variant X1
uncharacterized LOC123870873, transcript variant X2
uncharacterized protein LOC123870873 isoform X1
uncharacterized protein LOC123870873 isoform X2
acyl-coenzyme A diphosphatase NUDT19-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
STE20/SPS1-related proline-alanine-rich protein kinase
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
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
elongation factor 1-alpha, transcript variant X1
elongation factor 1-alpha, transcript variant X2
28S ribosomal protein S31, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and MYND domain-containing protein 1-like, transcript variant X1
ankyrin repeat and MYND domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ankyrin repeat and MYND domain-containing protein 1-like isoform X1
ankyrin repeat and MYND domain-containing protein 1-like isoform X2
PRL-1 phosphatase, transcript variant X3
PRL-1 phosphatase, transcript variant X1
PRL-1 phosphatase, transcript variant X2
PRL-1 phosphatase, transcript variant X4
proteasome inhibitor PI31 subunit, transcript variant X2
proteasome inhibitor PI31 subunit, transcript variant X1
kinesin-like protein KIF13B, transcript variant X1
kinesin-like protein KIF13B, transcript variant X3
kinesin-like protein KIF13B, transcript variant X6
kinesin-like protein KIF13B, transcript variant X7
kinesin-like protein KIF13B, transcript variant X8
kinesin-like protein KIF13B, transcript variant X9
kinesin-like protein KIF13B, transcript variant X10
kinesin-like protein KIF13B, transcript variant X4
kinesin-like protein KIF13B, transcript variant X13
kinesin-like protein KIF13B, transcript variant X11
kinesin-like protein KIF13B, transcript variant X12
kinesin-like protein KIF13B, transcript variant X2
kinesin-like protein KIF13B, 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 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, including 20 samples with support for all annotated introns
uncharacterized LOC123869925, transcript variant X3
uncharacterized protein LOC123869925 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123869925, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123869925, transcript variant X2
uncharacterized protein LOC123869925 isoform X1
uncharacterized protein LOC123869925 isoform 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
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
intraflagellar transport protein 74 homolog, transcript variant X2
intraflagellar transport protein 74 homolog, transcript variant X1
intraflagellar transport protein 74 homolog
leucine-rich PPR motif-containing protein, mitochondrial
uncharacterized LOC123878218, transcript variant X2
uncharacterized LOC123878218, transcript variant X1
uncharacterized protein LOC123878218 isoform X2
uncharacterized protein LOC123878218 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
solute carrier family 12 member 6, transcript variant X1
solute carrier family 12 member 6, transcript variant X5
solute carrier family 12 member 6, transcript variant X4
solute carrier family 12 member 6, transcript variant X2
solute carrier family 12 member 6 isoform X1
solute carrier family 12 member 4 isoform X4
solute carrier family 12 member 4 isoform X3
monocarboxylate transporter 1-like, transcript variant X2
monocarboxylate transporter 1-like, transcript variant X1
monocarboxylate transporter 1-like isoform X2
monocarboxylate transporter 1-like isoform X1
monocarboxylate transporter 9-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 1 sample with support for all annotated introns
monocarboxylate transporter 9-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 12 samples with support for all annotated introns
trypsin CFT-1-like, transcript variant X1
trypsin CFT-1-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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 194 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: 154 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: 168 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 12 member 6, transcript variant X3
solute carrier family 12 member 6 isoform X2
FAST kinase domain-containing protein 2, mitochondrial-like
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X3
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X2
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X1
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like isoform X1
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X5
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X6
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like, transcript variant X4
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like isoform X2
ornithine aminotransferase, mitochondrial, transcript variant X1
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 6 samples with support for all annotated introns
ornithine aminotransferase, mitochondrial, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ornithine aminotransferase, mitochondrial, transcript variant X6
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 5 samples with support for all annotated introns
ornithine aminotransferase, mitochondrial, transcript variant X3
ornithine aminotransferase, mitochondrial, transcript variant X2
ornithine aminotransferase, mitochondrial, transcript variant X9
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 7 samples with support for all annotated introns
ornithine aminotransferase, mitochondrial, transcript variant X4
ornithine aminotransferase, mitochondrial, 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 2 samples with support for all annotated introns
ornithine aminotransferase, mitochondrial, transcript variant X7
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 3 samples with support for all annotated introns
ornithine aminotransferase, mitochondrial isoform X3
ornithine aminotransferase, mitochondrial isoform X2
ornithine aminotransferase, mitochondrial isoform X1
ornithine aminotransferase, mitochondrial isoform X4
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2, transcript variant X2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2, transcript variant X1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2, transcript variant X3
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2 isoform X1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2 isoform X2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 5
E3 ubiquitin-protein ligase Topors, transcript variant X1
E3 ubiquitin-protein ligase Topors, transcript variant X3
E3 ubiquitin-protein ligase Topors, transcript variant X2
E3 ubiquitin-protein ligase Topors isoform X1
E3 ubiquitin-protein ligase Topors isoform X2
mitogen-activated protein kinase p38b, transcript variant X2
mitogen-activated protein kinase p38b, transcript variant X1
mitogen-activated protein kinase p38b isoform X2
mitogen-activated protein kinase p38b isoform X1
doublesex- and mab-3-related transcription factor 2-like, transcript variant X2
doublesex- and mab-3-related transcription factor 2-like, transcript variant X1
doublesex- and mab-3-related transcription factor 2-like isoform X2
doublesex- and mab-3-related transcription factor 2-like isoform X1
DNA ligase 4-like, transcript variant X1
DNA ligase 4-like, transcript variant X3
DNA ligase 4-like, transcript variant X2
F-box/WD repeat-containing protein 9-like, transcript variant X3
F-box/WD repeat-containing protein 9-like, transcript variant X1
F-box/WD repeat-containing protein 9-like, transcript variant X2
F-box/WD repeat-containing protein 9-like
alpha/beta hydrolase domain-containing protein 17B
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
ESX-1 secretion-associated protein EspK-like
lipid droplet-associated hydrolase, transcript variant X1
lipid droplet-associated hydrolase, transcript variant X2
THAP domain-containing protein 1-like, transcript variant X1
THAP domain-containing protein 1-like, transcript variant X2
zinc finger protein 677-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 4 samples with support for all annotated introns
zinc finger protein 677-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 12 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
protein rolling stone-like, transcript variant X1
protein rolling stone-like, transcript variant X2
voltage-dependent calcium channel subunit alpha-2/delta-3
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X13
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X1
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X3
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X4
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X2
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X5
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X6
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X7
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X9
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X8
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X10
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X11
voltage-dependent calcium channel subunit alpha-2/delta-3, transcript variant X12
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X1
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X3
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X4
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X6
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X7
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X9
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X10
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X2
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X5
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X8
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X11
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X12
voltage-dependent calcium channel subunit alpha-2/delta-3 isoform X13
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 27 samples with support for all annotated introns
fork head domain-containing protein FD4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fork head domain-containing protein FD4-like, transcript variant X2
fork head domain-containing protein FD4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
electron transfer flavoprotein subunit alpha, mitochondrial
alkaline ceramidase, transcript variant X1
alkaline ceramidase, transcript variant X2
uncharacterized LOC123875772, transcript variant X1
uncharacterized LOC123875772, transcript variant X2
lipoyltransferase 1, mitochondrial, transcript variant X1
lipoyltransferase 1, mitochondrial, transcript variant X2
lipoyltransferase 1, mitochondrial isoform X1
lipoyltransferase 1, mitochondrial isoform X2
uncharacterized LOC123875724, transcript variant X2
uncharacterized protein LOC123875724 isoform X2
uncharacterized LOC123875724, transcript variant X1
uncharacterized protein LOC123875724 isoform X1
leucine-rich repeat transmembrane neuronal protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
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
UPF0489 protein C5orf22 homolog, transcript variant X1
UPF0489 protein C5orf22 homolog, transcript variant X2
insulin-like receptor, transcript variant X1
insulin-like receptor, transcript variant X2
insulin-like receptor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
insulin-like receptor, transcript variant X4
glycosaminoglycan xylosylkinase homolog, transcript variant X3
glycosaminoglycan xylosylkinase homolog, transcript variant X2
glycosaminoglycan xylosylkinase homolog, transcript variant X1
glycosaminoglycan xylosylkinase homolog, transcript variant X4
glycosaminoglycan xylosylkinase homolog isoform X4
glycosaminoglycan xylosylkinase homolog isoform X3
glycosaminoglycan xylosylkinase homolog isoform X1
glycosaminoglycan xylosylkinase homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitochondrial import receptor subunit TOM40 homolog
receptor-interacting serine/threonine-protein kinase 1-like
mitochondrial enolase superfamily member 1-like, transcript variant X1
mitochondrial enolase superfamily member 1-like, transcript variant X2
mitochondrial enolase superfamily member 1-like isoform X1
mitochondrial enolase superfamily member 1-like isoform X2
WD repeat and HMG-box DNA-binding protein 1, transcript variant X1
WD repeat and HMG-box DNA-binding protein 1 isoform X1
WD repeat and HMG-box DNA-binding protein 1, transcript variant X2
WD repeat and HMG-box DNA-binding protein 1 isoform X2
cystathionine gamma-lyase, transcript variant X2
cystathionine gamma-lyase, transcript variant X1
cystathionine gamma-lyase, transcript variant X3
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase-like
probable RNA helicase armi, transcript variant X2
probable RNA helicase armi, transcript variant X1
cytosolic carboxypeptidase 1-like, transcript variant X2
cytosolic carboxypeptidase 1-like, transcript variant X1
cytosolic carboxypeptidase 1-like, transcript variant X4
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
uncharacterized LOC123876858, transcript variant X1
uncharacterized LOC123876858, transcript variant X2
uncharacterized LOC123876858, 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 7 samples with support for all annotated introns
uncharacterized LOC123876858, transcript variant X4
uncharacterized protein LOC123876858 isoform X1
uncharacterized protein LOC123876858 isoform X2
uncharacterized protein LOC123876858 isoform X3
uncharacterized protein LOC123876858 isoform X4
adhesion G-protein coupled receptor G2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
neuronal acetylcholine receptor subunit alpha-10-like, transcript variant X2
neuronal acetylcholine receptor subunit alpha-10-like, transcript variant X1
neuronal acetylcholine receptor subunit alpha-10-like isoform X2
neuronal acetylcholine receptor subunit alpha-10-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cyclin-dependent kinase 10, transcript variant X2
cyclin-dependent kinase 10, transcript variant X1
methionine aminopeptidase 1D, mitochondrial, transcript variant X3
methionine aminopeptidase 1D, mitochondrial, 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
methionine aminopeptidase 1D, mitochondrial, transcript variant X4
methionine aminopeptidase 1D, mitochondrial, transcript variant X2
methionine aminopeptidase 1D, mitochondrial isoform X2
methionine aminopeptidase 1D, mitochondrial isoform X1
methionine aminopeptidase 1D, mitochondrial isoform X3
protein N-terminal glutamine amidohydrolase
pancreatic lipase-related protein 2-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 72% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123871118, transcript variant X3
uncharacterized LOC123871118, transcript variant X1
uncharacterized LOC123871118, 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 4 samples with support for all annotated introns
uncharacterized LOC123871130, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123871130, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
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
glycine-rich protein-like, transcript variant X1
glycine-rich protein-like, transcript variant X2
uncharacterized LOC123873940, transcript variant X1
uncharacterized LOC123873940, 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
uncharacterized LOC123873940, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized protein LOC123873940 isoform X2
uncharacterized protein LOC123873940 isoform X1
solute carrier organic anion transporter family member 5A1-like, transcript variant X1
solute carrier organic anion transporter family member 5A1-like, transcript variant X2
solute carrier organic anion transporter family member 5A1-like
peptidyl-prolyl cis-trans isomerase-like, transcript variant X1
peptidyl-prolyl cis-trans isomerase-like, transcript variant X2
peptidyl-prolyl cis-trans isomerase-like
mitochondrial ribonuclease P protein 1 homolog
uncharacterized LOC123876092, transcript variant X2
uncharacterized LOC123876092, transcript variant X1
uncharacterized protein LOC123876092 isoform X2
uncharacterized protein LOC123876092 isoform X1
eukaryotic translation initiation factor 3 subunit E
zinc finger protein 480-like, transcript variant X2
zinc finger protein 480-like, transcript variant X1
uncharacterized protein LOC123876127 isoform X2
39S ribosomal protein L53, mitochondrial
protein argonaute-2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 121 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein argonaute-2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 116 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein ALP1-like, transcript variant X1
protein ALP1-like, transcript variant X2
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like isoform X2
tumor protein D54, 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 17 samples with support for all annotated introns
tumor protein D54, 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 4 samples with support for all annotated introns
tumor protein D54, transcript variant X2
uncharacterized protein LOC123877407 isoform X2
proteasomal ubiquitin receptor ADRM1, transcript variant X3
proteasomal ubiquitin receptor ADRM1, transcript variant X1
proteasomal ubiquitin receptor ADRM1, transcript variant X2
proteasomal ubiquitin receptor ADRM1 isoform X1
proteasomal ubiquitin receptor ADRM1 isoform X2
proteasomal ubiquitin receptor ADRM1 isoform X3
uncharacterized LOC123875952, transcript variant X2
uncharacterized LOC123875952, transcript variant X1
uncharacterized LOC123875952, transcript variant X3
uncharacterized LOC123875952, transcript variant X4
uncharacterized LOC123875952, transcript variant X5
uncharacterized LOC123875952, transcript variant X6
uncharacterized protein LOC123875952 isoform X1
uncharacterized protein LOC123875952 isoform X2
uncharacterized protein LOC123875952 isoform X4
uncharacterized protein LOC123875952 isoform X3
uncharacterized protein LOC123875952 isoform X5
DNA-directed RNA polymerases I, II, and III subunit RPABC4, transcript variant X2
DNA-directed RNA polymerases I, II, and III subunit RPABC4, transcript variant X1
DNA-directed RNA polymerases I, II, and III subunit RPABC4
nucleoside diphosphate kinase 7, transcript variant X2
nucleoside diphosphate kinase 7, 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 10 samples with support for all annotated introns
nucleoside diphosphate kinase 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123873684, 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 2 samples with support for all annotated introns
uncharacterized LOC123873684, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC123873684 isoform X1
uncharacterized protein LOC123873684 isoform X2
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
adenylyl cyclase-associated protein 1, transcript variant X3
adenylyl cyclase-associated protein 1, transcript variant X1
adenylyl cyclase-associated protein 1, transcript variant X4
adenylyl cyclase-associated protein 1, transcript variant X5
adenylyl cyclase-associated protein 1, transcript variant X2
adenylyl cyclase-associated protein 1 isoform X1
adenylyl cyclase-associated protein 1 isoform X2
adenylyl cyclase-associated protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transfer RNA asparagine (anticodon AUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nicotinate phosphoribosyltransferase, transcript variant X1
nicotinate phosphoribosyltransferase, transcript variant X2
nicotinate phosphoribosyltransferase isoform X2
nicotinate phosphoribosyltransferase isoform X1
zinc finger protein 251-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 251-like, transcript variant X1
transcriptional coactivator YAP1, transcript variant X6
transcriptional coactivator YAP1, transcript variant X7
transcriptional coactivator YAP1, transcript variant X2
transcriptional coactivator YAP1, transcript variant X4
transcriptional coactivator YAP1, transcript variant X3
transcriptional coactivator YAP1, transcript variant X5
transcriptional coactivator YAP1, transcript variant X1
transcriptional coactivator YAP1 isoform X1
transcriptional coactivator YAP1 isoform X3
transcriptional coactivator YAP1 isoform X2
WW domain-containing transcription regulator protein 1 isoform X6
WW domain-containing transcription regulator protein 1 isoform X7
transcriptional coactivator YAP1 isoform X4
transcriptional coactivator YAP1 isoform 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 4 samples with support for all annotated introns
myrosinase 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myrosinase 1-like, transcript variant X4
uncharacterized LOC123873922, transcript variant X2
uncharacterized LOC123873922, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutaminase kidney isoform, mitochondrial, transcript variant X7
glutaminase kidney isoform, mitochondrial isoform X7
glutaminase kidney isoform, mitochondrial, transcript variant X4
glutaminase kidney isoform, mitochondrial, transcript variant X6
glutaminase liver isoform, mitochondrial isoform X4
glutaminase liver isoform, mitochondrial isoform X6
glutaminase kidney isoform, mitochondrial, transcript variant X5
glutaminase kidney isoform, mitochondrial, transcript variant X3
glutaminase kidney isoform, mitochondrial, transcript variant X2
glutaminase kidney isoform, mitochondrial, transcript variant X1
glutaminase liver isoform, mitochondrial isoform X1
glutaminase liver isoform, mitochondrial isoform X3
glutaminase liver isoform, mitochondrial isoform X2
glutaminase liver isoform, mitochondrial isoform X5
28S ribosomal protein S28, mitochondrial
slit homolog 1 protein-like, transcript variant X2
slit homolog 1 protein-like, transcript variant X1
E3 ubiquitin-protein ligase MSL2, transcript variant X1
E3 ubiquitin-protein ligase MSL2, transcript variant X2
E3 ubiquitin-protein ligase MSL2, transcript variant X3
E3 ubiquitin-protein ligase MSL2 isoform X1
E3 ubiquitin-protein ligase MSL2 isoform X2
E3 ubiquitin-protein ligase MSL2 isoform X3
endoribonuclease CG2145-like, transcript variant X2
endoribonuclease CG2145-like, transcript variant X1
5'-nucleotidase domain-containing protein 3, transcript variant X1
5'-nucleotidase domain-containing protein 3, transcript variant X2
5'-nucleotidase domain-containing protein 3 isoform X1
5'-nucleotidase domain-containing protein 3 isoform X2
protein-cysteine N-palmitoyltransferase Rasp
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 21 samples with support for all annotated introns
DNA helicase MCM8, transcript variant X1
DNA helicase MCM8, 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 1 sample with support for all annotated introns
uncharacterized LOC123870822, transcript variant X2
uncharacterized LOC123870822, transcript variant X1
uncharacterized LOC123870822, transcript variant X3
zinc finger BED domain-containing protein 4-like
NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial-like
NADH dehydrogenase [ubiquinone] iron-sulfur protein 3, mitochondrial-like
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 49% coverage of the annotated genomic feature by RNAseq alignments
chromodomain-helicase-DNA-binding protein 1, transcript variant X5
chromodomain-helicase-DNA-binding protein 1, transcript variant X3
chromodomain-helicase-DNA-binding protein 1, transcript variant X4
chromodomain-helicase-DNA-binding protein 1, transcript variant X2
chromodomain-helicase-DNA-binding protein 1, transcript variant X1
chromodomain-helicase-DNA-binding protein 1 isoform X4
chromodomain-helicase-DNA-binding protein 1 isoform X2
chromodomain-helicase-DNA-binding protein 1 isoform X3
chromodomain-helicase-DNA-binding protein 1 isoform X1
CD2 antigen cytoplasmic tail-binding protein 2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
protein ANTAGONIST OF LIKE HETEROCHROMATIN PROTEIN 1-like
methyltransferase-like 26, transcript variant X2
methyltransferase-like 26, 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 27 samples with support for all annotated introns
GPI ethanolamine phosphate transferase 1
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
ras GTPase-activating-like protein IQGAP1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
cilia- and flagella-associated protein 57, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cilia- and flagella-associated protein 57, 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
cilia- and flagella-associated protein 57, transcript variant X3
cilia- and flagella-associated protein 57 isoform X2
cilia- and flagella-associated protein 57 isoform X1
cilia- and flagella-associated protein 57 isoform X3
probable very-long-chain enoyl-CoA reductase art-1
heat shock factor protein, transcript variant X4
heat shock factor protein, transcript variant X8
heat shock factor protein, transcript variant X1
heat shock factor protein, transcript variant X5
heat shock factor protein, transcript variant X2
heat shock factor protein, transcript variant X6
heat shock factor protein, transcript variant X3
heat shock factor protein, transcript variant X10
heat shock factor protein, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
heat shock factor protein, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
heat shock factor protein, transcript variant X7
heat shock factor protein, transcript variant X12
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 22 samples with support for all annotated introns
dynein regulatory complex subunit 6-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 23 samples with support for all annotated introns
phenoloxidase-activating factor 2-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 4 samples with support for all annotated introns
phenoloxidase-activating factor 2-like, transcript variant X1
phenoloxidase-activating factor 2-like isoform X2
phenoloxidase-activating factor 2-like isoform 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 15 samples with support for all annotated introns
long-chain-fatty-acid--CoA ligase ACSBG2-like, transcript variant X1
long-chain-fatty-acid--CoA ligase ACSBG2-like, transcript variant X2
very long-chain-fatty-acid--CoA ligase bubblegum-like isoform X1
long-chain-fatty-acid--CoA ligase ACSBG2-like isoform X2
long-chain-fatty-acid--CoA ligase ACSBG2-like, transcript variant X3
long-chain-fatty-acid--CoA ligase ACSBG2-like isoform X3
zinc finger protein 532-like, transcript variant X2
zinc finger protein 532-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 532-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
myb-like protein X, transcript variant X3
myb-like protein X, transcript variant X2
myb-like protein X, transcript variant X1
cilia- and flagella-associated protein 161, transcript variant X1
cilia- and flagella-associated protein 161, transcript variant X3
cilia- and flagella-associated protein 161, transcript variant X2
cilia- and flagella-associated protein 161 isoform X1
cilia- and flagella-associated protein 161 isoform X3
cilia- and flagella-associated protein 161 isoform X2
cilia- and flagella-associated protein 161-like, transcript variant X1
cilia- and flagella-associated protein 161-like, transcript variant X3
cilia- and flagella-associated protein 161-like, transcript variant X2
cilia- and flagella-associated protein 161-like isoform X1
cilia- and flagella-associated protein 161-like isoform X3
uncharacterized protein LOC123872038 isoform X2
band 4.1-like protein 4, transcript variant X1
band 4.1-like protein 4, transcript variant X2
band 4.1-like protein 4, transcript variant X3
serine/arginine repetitive matrix protein 1-like, transcript variant X4
serine/arginine repetitive matrix protein 1-like, transcript variant X2
serine/arginine repetitive matrix protein 1-like, transcript variant X3
serine/arginine repetitive matrix protein 1-like, transcript variant X1
serine/arginine repetitive matrix protein 1-like isoform X1
serine/arginine repetitive matrix protein 1-like isoform X2
neuronal acetylcholine receptor subunit alpha-7, transcript variant X1
neuronal acetylcholine receptor subunit alpha-7, transcript variant X2
neuronal acetylcholine receptor subunit alpha-7 isoform X1
neuronal acetylcholine receptor subunit alpha-7 isoform X2
acetylcholine receptor subunit beta-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB1
potential E3 ubiquitin-protein ligase ariadne-2
ATP-dependent 6-phosphofructokinase, transcript variant X1
ATP-dependent 6-phosphofructokinase, transcript variant X3
ATP-dependent 6-phosphofructokinase, transcript variant X2
ATP-dependent 6-phosphofructokinase isoform X1
ATP-dependent 6-phosphofructokinase isoform X3
ATP-dependent 6-phosphofructokinase isoform X2
ATP-dependent 6-phosphofructokinase, transcript variant X4
ATP-dependent 6-phosphofructokinase isoform X4
translocating chain-associated membrane protein 1
putative cyclin-dependent serine/threonine-protein kinase DDB_G0272797/DDB_G0274007
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized transmembrane protein DDB_G0289901-like, transcript variant X2
uncharacterized transmembrane protein DDB_G0289901-like, transcript variant X1
uncharacterized transmembrane protein DDB_G0289901-like isoform X2
uncharacterized transmembrane protein DDB_G0289901-like isoform X1
serrate RNA effector molecule homolog, transcript variant X2
serrate RNA effector molecule homolog, transcript variant X1
serrate RNA effector molecule homolog isoform X1
serrate RNA effector molecule homolog, transcript variant X3
serrate RNA effector molecule homolog isoform X2
uncharacterized LOC123872631, transcript variant X2
uncharacterized LOC123872631, transcript variant X3
uncharacterized LOC123872631, 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
sphingomyelin phosphodiesterase, transcript variant X2
sphingomyelin phosphodiesterase, transcript variant X3
sphingomyelin phosphodiesterase, transcript variant X1
sphingomyelin phosphodiesterase, transcript variant X4
sphingomyelin phosphodiesterase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sphingomyelin phosphodiesterase isoform X1
sphingomyelin phosphodiesterase isoform X3
sphingomyelin phosphodiesterase isoform X4
sphingomyelin phosphodiesterase isoform X5
sphingomyelin phosphodiesterase isoform X2
oocyte zinc finger protein XlCOF6-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 8 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6-like isoform X1
delta and Notch-like epidermal growth factor-related receptor, transcript variant X1
delta and Notch-like epidermal growth factor-related receptor, transcript variant X3
delta and Notch-like epidermal growth factor-related receptor, transcript variant X2
delta and Notch-like epidermal growth factor-related receptor isoform X1
delta and Notch-like epidermal growth factor-related receptor isoform X2
protein grainyhead, transcript variant X3
protein grainyhead, transcript variant X2
protein grainyhead, transcript variant X1
cytoplasmic tRNA 2-thiolation protein 2, transcript variant X2
cytoplasmic tRNA 2-thiolation protein 2, transcript variant X1
cytoplasmic tRNA 2-thiolation protein 2 isoform X1
probable elongation factor 1-delta, transcript variant X3
probable elongation factor 1-delta, transcript variant X2
probable elongation factor 1-delta, transcript variant X4
probable elongation factor 1-delta, transcript variant X1
probable elongation factor 1-delta, transcript variant X6
probable elongation factor 1-delta, transcript variant X5
probable elongation factor 1-delta isoform X1
probable elongation factor 1-delta isoform X2
cytoplasmic tRNA 2-thiolation protein 2 isoform X2
casein kinase II subunit alpha, transcript variant X2
casein kinase II subunit alpha, transcript variant X1
trafficking protein particle complex subunit 8
aryl hydrocarbon receptor nuclear translocator homolog
tudor domain-containing protein 7, transcript variant X1
tudor domain-containing protein 7, transcript variant X3
tudor domain-containing protein 7, transcript variant X2
glycylpeptide N-tetradecanoyltransferase 2
60S ribosomal protein L13, transcript variant X2
60S ribosomal protein L13, transcript variant X1
zinc finger protein on ecdysone puffs, transcript variant X3
zinc finger protein on ecdysone puffs, transcript variant X1
zinc finger protein on ecdysone puffs, transcript variant X2
zinc finger protein on ecdysone puffs, transcript variant X4
zinc finger protein on ecdysone puffs isoform X2
zinc finger protein on ecdysone puffs isoform X1
zinc finger protein on ecdysone puffs isoform X3
uncharacterized LOC123875395, transcript variant X1
uncharacterized LOC123875395, transcript variant X3
uncharacterized LOC123875395, transcript variant X2
uncharacterized LOC123875395, transcript variant X4
probable leucine--tRNA ligase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
FUN14 domain-containing protein 1A-like, transcript variant X1
FUN14 domain-containing protein 1A-like, transcript variant X2
FUN14 domain-containing protein 1A-like isoform X1
FUN14 domain-containing protein 1A-like isoform X2
uncharacterized LOC123875365, transcript variant X2
uncharacterized LOC123875365, transcript variant X1
uncharacterized protein LOC123875365 isoform X2
uncharacterized protein LOC123875365 isoform X1
nuclear speckle splicing regulatory protein 1
negative elongation factor D, transcript variant X1
negative elongation factor D, transcript variant X2
potassium voltage-gated channel subfamily KQT member 5, transcript variant X3
potassium voltage-gated channel subfamily KQT member 5, transcript variant X1
potassium voltage-gated channel subfamily KQT member 5, transcript variant X6
potassium voltage-gated channel subfamily KQT member 5, transcript variant X9
potassium voltage-gated channel subfamily KQT member 5, transcript variant X11
potassium voltage-gated channel subfamily KQT member 5, transcript variant X10
potassium voltage-gated channel subfamily KQT member 1 isoform X3
potassium voltage-gated channel subfamily KQT member 1 isoform X1
potassium voltage-gated channel subfamily KQT member 1 isoform X10
potassium voltage-gated channel subfamily KQT member 1 isoform X9
potassium voltage-gated channel subfamily KQT member 5, transcript variant X2
potassium voltage-gated channel subfamily KQT member 5, transcript variant X5
potassium voltage-gated channel subfamily KQT member 5, transcript variant X12
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 2 samples with support for all annotated introns
potassium voltage-gated channel subfamily KQT member 5, transcript variant X4
potassium voltage-gated channel subfamily KQT member 5, transcript variant X7
potassium voltage-gated channel subfamily KQT member 5, transcript variant X8
potassium voltage-gated channel subfamily KQT member 1 isoform X2
potassium voltage-gated channel subfamily KQT member 1 isoform X5
potassium voltage-gated channel subfamily KQT member 1 isoform X4
potassium voltage-gated channel subfamily KQT member 1 isoform X7
potassium voltage-gated channel subfamily KQT member 1 isoform X8
potassium voltage-gated channel subfamily KQT member 5 isoform X11
potassium voltage-gated channel subfamily KQT member 1 isoform X6
potassium voltage-gated channel subfamily KQT member 5, transcript variant X13
potassium voltage-gated channel subfamily KQT member 5 isoform X12
survival of motor neuron-related-splicing factor 30
uncharacterized LOC123877530, transcript variant X1
uncharacterized LOC123877530, transcript variant X2
general odorant-binding protein 83a-like
gamma-interferon-inducible lysosomal thiol reductase-like, transcript variant X1
gamma-interferon-inducible lysosomal thiol reductase-like, transcript variant X2
gamma-interferon-inducible lysosomal thiol reductase-like isoform X1
gamma-interferon-inducible lysosomal thiol reductase-like isoform X2
splicing factor 45, transcript variant X2
splicing factor 45, 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 12 samples with support for all annotated introns
serine/threonine-protein kinase greatwall, transcript variant X2
serine/threonine-protein kinase greatwall, transcript variant X1
serine/threonine-protein kinase greatwall, transcript variant X3
serine/threonine-protein kinase greatwall isoform X1
serine/threonine-protein kinase greatwall isoform X2
circadian clock-controlled protein daywake-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
circadian clock-controlled protein daywake-like, transcript variant X1
circadian clock-controlled protein daywake-like
phosphatidylinositol glycan anchor biosynthesis class U protein
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
facilitated trehalose transporter Tret1-like
facilitated trehalose transporter Tret1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
uncharacterized LOC123872922, transcript variant X2
uncharacterized LOC123872922, transcript variant X1
uncharacterized protein LOC123872922 isoform X1
uncharacterized protein LOC123872922 isoform X2
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
phospholipid scramblase 2, transcript variant X2
phospholipid scramblase 2, transcript variant X1
phospholipid scramblase 2, transcript variant X8
phospholipid scramblase 2, transcript variant X3
uncharacterized protein LOC123873000 isoform X1
phospholipid scramblase 2, transcript variant X6
phospholipid scramblase 2, transcript variant X5
phospholipid scramblase 2, transcript variant X4
uncharacterized protein LOC123873000 isoform X2
phospholipid scramblase 2, transcript variant X7
uncharacterized protein LOC123873000 isoform X3
regulator of microtubule dynamics protein 1-like, transcript variant X2
regulator of microtubule dynamics protein 1-like, transcript variant X3
regulator of microtubule dynamics protein 1-like, transcript variant X1
regulator of microtubule dynamics protein 1-like, transcript variant X4
regulator of microtubule dynamics protein 1-like isoform X2
regulator of microtubule dynamics protein 1-like isoform X3
regulator of microtubule dynamics protein 1-like isoform X1
regulator of microtubule dynamics protein 1-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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% 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: 14 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: 10 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123877706, transcript variant X2
uncharacterized LOC123877706, transcript variant X1
uncharacterized LOC123877672, transcript variant X1
uncharacterized protein LOC123877672 isoform X1
uncharacterized LOC123877672, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein LOC123877672 isoform 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
C-type mannose receptor 2-like, transcript variant X3
C-type mannose receptor 2-like, transcript variant X2
C-type mannose receptor 2-like, transcript variant X1
C-type mannose receptor 2-like isoform X1
C-type mannose receptor 2-like isoform X2
sodium-dependent noradrenaline transporter-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
integrator complex subunit 6-B, transcript variant X1
integrator complex subunit 6-B, transcript variant X2
integrator complex subunit 6-B isoform 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 2 samples with support for all annotated introns
uncharacterized protein LOC123873335 isoform X2
hydroxymethylglutaryl-CoA lyase, mitochondrial, transcript variant X1
hydroxymethylglutaryl-CoA lyase, mitochondrial, transcript variant X2
hydroxymethylglutaryl-CoA lyase, mitochondrial isoform X1
hydroxymethylglutaryl-CoA lyase, mitochondrial isoform 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 27 samples with support for all annotated introns
putative WEB family protein At1g65010, chloroplastic, transcript variant X1
putative WEB family protein At1g65010, chloroplastic, transcript variant X2
putative WEB family protein At1g65010, chloroplastic, transcript variant X3
putative WEB family protein At1g65010, chloroplastic, transcript variant X4
putative WEB family protein At1g65010, chloroplastic isoform X1
putative WEB family protein At1g65010, chloroplastic isoform X2
cullin-associated NEDD8-dissociated protein 1
probable ATP-dependent RNA helicase Dbp73D
uncharacterized LOC123873293, transcript variant X2
uncharacterized LOC123873293, transcript variant X1
uncharacterized LOC123873293, transcript variant X3
histone-lysine N-methyltransferase, H3 lysine-79 specific, transcript variant X2
histone-lysine N-methyltransferase, H3 lysine-79 specific, transcript variant X1
histone-lysine N-methyltransferase, H3 lysine-79 specific isoform X2
histone-lysine N-methyltransferase, H3 lysine-79 specific isoform X1
ankyrin repeat domain-containing protein 49, transcript variant X5
ankyrin repeat domain-containing protein 49, transcript variant X3
ankyrin repeat domain-containing protein 49, transcript variant X2
ankyrin repeat domain-containing protein 49, transcript variant X1
ankyrin repeat domain-containing protein 49, transcript variant X4
ankyrin repeat domain-containing protein 49
A disintegrin and metalloproteinase with thrombospondin motifs 14-like
14-3-3 protein zeta, transcript variant X3
14-3-3 protein zeta, transcript variant X1
14-3-3 protein zeta, transcript variant X2
14-3-3 protein zeta, transcript variant X4
phosphatidate phosphatase LPIN2, transcript variant X2
phosphatidate phosphatase LPIN2, transcript variant X1
phosphatidate phosphatase LPIN2, transcript variant X4
phosphatidate phosphatase LPIN2 isoform X2
phosphatidate phosphatase LPIN2 isoform X1
phosphatidate phosphatase LPIN2, transcript variant X3
uncharacterized LOC123873956, transcript variant X1
uncharacterized LOC123873956, transcript variant X2
uncharacterized protein LOC123873956 isoform X1
uncharacterized protein LOC123873956 isoform X2
major facilitator superfamily domain-containing protein 12-like
ubiquitin carboxyl-terminal hydrolase isozyme L3-like
aspartyl/asparaginyl beta-hydroxylase, transcript variant X3
aspartyl/asparaginyl beta-hydroxylase, transcript variant X2
aspartyl/asparaginyl beta-hydroxylase, transcript variant X1
aspartyl/asparaginyl beta-hydroxylase, transcript variant X5
aspartyl/asparaginyl beta-hydroxylase, transcript variant X4
aspartyl/asparaginyl beta-hydroxylase isoform X3
aspartyl/asparaginyl beta-hydroxylase isoform X4
aspartyl/asparaginyl beta-hydroxylase isoform X2
aspartyl/asparaginyl beta-hydroxylase isoform X1
metallo-beta-lactamase domain-containing protein 1, transcript variant X1
metallo-beta-lactamase domain-containing protein 1, transcript variant X2
metallo-beta-lactamase domain-containing protein 1 isoform X1
metallo-beta-lactamase domain-containing protein 1 isoform X2
sodium/hydrogen exchanger 7, transcript variant X6
sodium/hydrogen exchanger 7, transcript variant X1
sodium/hydrogen exchanger 7, transcript variant X2
sodium/hydrogen exchanger 7, transcript variant X11
sodium/hydrogen exchanger 7, transcript variant X12
sodium/hydrogen exchanger 7, transcript variant X5
sodium/hydrogen exchanger 7, transcript variant X7
sodium/hydrogen exchanger 7, transcript variant X8
sodium/hydrogen exchanger 7, transcript variant X9
sodium/hydrogen exchanger 7, transcript variant X10
sodium/hydrogen exchanger 7, transcript variant X3
sodium/hydrogen exchanger 7, transcript variant X4
sodium/hydrogen exchanger 7, transcript variant X13
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 26 samples with support for all annotated introns
low-density lipoprotein receptor, transcript variant X16
low-density lipoprotein receptor, 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 19 samples with support for all annotated introns
low-density lipoprotein receptor, transcript variant X5
low-density lipoprotein receptor, transcript variant X2
low-density lipoprotein receptor, transcript variant X4
low-density lipoprotein receptor, transcript variant X6
low-density lipoprotein receptor, transcript variant X1
very low-density lipoprotein receptor isoform X10
low-density lipoprotein receptor isoform X2
very low-density lipoprotein receptor isoform X5
very low-density lipoprotein receptor isoform X1
very low-density lipoprotein receptor isoform X4
very low-density lipoprotein receptor isoform X6
very low-density lipoprotein receptor isoform X3
low-density lipoprotein receptor, transcript variant X10
low-density lipoprotein receptor, transcript variant X13
low-density lipoprotein receptor, transcript variant X14
low-density lipoprotein receptor, transcript variant X7
low-density lipoprotein receptor, transcript variant X15
low-density lipoprotein receptor, transcript variant X9
low-density lipoprotein receptor, transcript variant X11
low-density lipoprotein receptor, transcript variant X8
low-density lipoprotein receptor, transcript variant X12
low-density lipoprotein receptor isoform X8
low-density lipoprotein receptor isoform X7
low-density lipoprotein receptor-related protein 8 isoform X9
queuine tRNA-ribosyltransferase accessory subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 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: 59 Proteins, and 78% 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: 14 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: 6 Proteins
N-alpha-acetyltransferase 35, NatC auxiliary subunit, 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
N-alpha-acetyltransferase 35, NatC auxiliary subunit, 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 13 samples with support for all annotated introns
N-alpha-acetyltransferase 35, NatC auxiliary subunit isoform X1
N-alpha-acetyltransferase 35, NatC auxiliary subunit isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123871347, transcript variant X2
uncharacterized LOC123871347, transcript variant X1
uncharacterized protein LOC123871347 isoform X2
uncharacterized protein LOC123871347 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 72% 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 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 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: 39 Proteins, 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: 45 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: 50 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
sodium-coupled monocarboxylate transporter 1-like
sodium-coupled monocarboxylate transporter 1-like, transcript variant X1
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 5 samples with support for all annotated introns
sodium-coupled monocarboxylate transporter 1-like isoform X1
sodium-coupled monocarboxylate transporter 1-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 13 samples with support for all annotated introns
sodium-coupled monocarboxylate transporter 1-like isoform X2
sequestosome-1-like, transcript variant X2
sequestosome-1-like, transcript variant X3
sequestosome-1-like, transcript variant X5
sequestosome-1-like, transcript variant X4
sequestosome-1-like, transcript variant X1
uncharacterized protein LOC123876738 isoform X2
biogenesis of lysosome-related organelles complex 1 subunit 5
arfGAP with SH3 domain, ANK repeat and PH domain-containing protein, transcript variant X1
arfGAP with SH3 domain, ANK repeat and PH domain-containing protein, transcript variant X3
arfGAP with SH3 domain, ANK repeat and PH domain-containing protein, transcript variant X2
arfGAP with SH3 domain, ANK repeat and PH domain-containing protein, transcript variant X5
arfGAP with SH3 domain, ANK repeat and PH domain-containing protein, transcript variant X4
arfGAP with SH3 domain, ANK repeat and PH domain-containing protein isoform X1
arfGAP with SH3 domain, ANK repeat and PH domain-containing protein isoform X3
arfGAP with SH3 domain, ANK repeat and PH domain-containing protein isoform X2
arfGAP with SH3 domain, ANK repeat and PH domain-containing protein isoform X4
arfGAP with SH3 domain, ANK repeat and PH domain-containing protein isoform X5
probable hydroxyacid-oxoacid transhydrogenase, mitochondrial, transcript variant X2
probable hydroxyacid-oxoacid transhydrogenase, mitochondrial, transcript variant X1
probable hydroxyacid-oxoacid transhydrogenase, mitochondrial isoform X1
probable hydroxyacid-oxoacid transhydrogenase, mitochondrial isoform X2
toll-like receptor Tollo, transcript variant X1
toll-like receptor Tollo, transcript variant X3
toll-like receptor Tollo, transcript variant X2
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
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
homeobox protein dve-1, transcript variant X2
homeobox protein dve-1, transcript variant X3
homeobox protein dve-1, transcript variant X1
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon CGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
thyroid hormone-inducible hepatic protein
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
serine/arginine repetitive matrix protein 1-like
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00618
lysine-specific demethylase 6A, transcript variant X1
lysine-specific demethylase 6A, transcript variant X2
lysine-specific demethylase 6A isoform X1
lysine-specific demethylase 6A isoform X2
dual specificity protein phosphatase 13-like, transcript variant X2
dual specificity protein phosphatase 13-like, transcript variant X1
dual specificity protein phosphatase 13-like, transcript variant X3
dual specificity protein phosphatase 13-like isoform X1
dual specificity protein phosphatase 13-like isoform X2
cleft lip and palate transmembrane protein 1-like protein
uncharacterized LOC123878114, transcript variant X2
uncharacterized LOC123878114, transcript variant X1
uncharacterized LOC123878114, transcript variant X3
uncharacterized protein LOC123878114 isoform X2
uncharacterized protein LOC123878114 isoform X1
uncharacterized protein LOC123878114 isoform X3
uncharacterized LOC123878130, transcript variant X2
uncharacterized LOC123878130, transcript variant X3
uncharacterized LOC123878130, transcript variant X1
uncharacterized protein LOC123878130 isoform X2
uncharacterized protein LOC123878130 isoform X1
uncharacterized protein LOC123878130 isoform 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
uncharacterized LOC123877031, transcript variant X3
uncharacterized LOC123877031, transcript variant X2
uncharacterized LOC123877031, transcript variant X1
uncharacterized protein LOC123877031 isoform X3
uncharacterized protein LOC123877031 isoform X2
uncharacterized protein LOC123877031 isoform X1
mediator of RNA polymerase II transcription subunit 30, transcript variant X1
mediator of RNA polymerase II transcription subunit 30, transcript variant X2
mediator of RNA polymerase II transcription subunit 30 isoform X1
mediator of RNA polymerase II transcription subunit 30 isoform X2
glycine-rich protein DOT1-like, transcript variant X2
glycine-rich protein DOT1-like, transcript variant X1
glycine-rich protein DOT1-like isoform X2
glycine-rich protein DOT1-like isoform X1
uncharacterized LOC123874990, transcript variant X1
uncharacterized LOC123874990, transcript variant X3
uncharacterized LOC123874990, transcript variant X2
uncharacterized protein LOC123874990 isoform X1
uncharacterized protein LOC123874990 isoform X3
uncharacterized protein LOC123874990 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 10 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 22 samples with support for all annotated introns
uncharacterized LOC123874970, transcript variant X1
uncharacterized LOC123874970, transcript variant X2
uncharacterized protein LOC123874970 isoform X1
uncharacterized protein LOC123874970 isoform X2
transfer RNA lysine (anticodon CUU); 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
glycogenin-2-like, transcript variant X9
glycogenin-2-like, transcript variant X2
glycogenin-2-like, transcript variant X1
glycogenin-2-like, 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 13 samples with support for all annotated introns
glycogenin-2-like, transcript variant X6
glycogenin-2-like, 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 25 samples with support for all annotated introns
glycogenin-2-like, transcript variant X3
glycogenin-2-like, transcript variant X7
glycogenin-2-like, 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 14 samples with support for all annotated introns
guanine nucleotide exchange factor DBS-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
guanine nucleotide exchange factor DBS-like, transcript variant X6
guanine nucleotide exchange factor DBS-like, transcript variant X7
guanine nucleotide exchange factor DBS-like, transcript variant X1
guanine nucleotide exchange factor DBS-like isoform X1
guanine nucleotide exchange factor DBS-like isoform X5
uncharacterized LOC123874911, transcript variant X2
uncharacterized LOC123874911, transcript variant X1
uncharacterized protein LOC123874911 isoform X1
uncharacterized protein LOC123874911 isoform X2
guanine nucleotide exchange factor DBS-like, transcript variant X4
guanine nucleotide exchange factor DBS-like isoform X4
guanine nucleotide exchange factor DBS-like, transcript variant X3
guanine nucleotide exchange factor DBS-like isoform X3
guanine nucleotide exchange factor DBS-like, transcript variant X2
guanine nucleotide exchange factor DBS-like isoform X2
E3 ubiquitin-protein ligase CCNB1IP1-like
double-stranded RNA-binding protein Staufen homolog 2, 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 5 samples with support for all annotated introns
double-stranded RNA-binding protein Staufen homolog 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
double-stranded RNA-binding protein Staufen homolog 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
double-stranded RNA-binding protein Staufen homolog 2, transcript variant X3
double-stranded RNA-binding protein Staufen homolog 2 isoform X1
double-stranded RNA-binding protein Staufen homolog 2 isoform X2
double-stranded RNA-binding protein Staufen homolog 2 isoform X4
double-stranded RNA-binding protein Staufen homolog 2 isoform X3
double-stranded RNA-binding protein Staufen homolog 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
double-stranded RNA-binding protein Staufen homolog 2 isoform X5
prolyl endopeptidase, transcript variant X1
prolyl endopeptidase, transcript variant X2
PAS domain-containing serine/threonine-protein kinase, transcript variant X2
PAS domain-containing serine/threonine-protein kinase, transcript variant X1
PAS domain-containing serine/threonine-protein kinase isoform X2
PAS domain-containing serine/threonine-protein kinase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
myocyte-specific enhancer factor 2, transcript variant X12
myocyte-specific enhancer factor 2, transcript variant X14
myocyte-specific enhancer factor 2, transcript variant X4
myocyte-specific enhancer factor 2, transcript variant X10
myocyte-specific enhancer factor 2, transcript variant X8
myocyte-specific enhancer factor 2, transcript variant X2
myocyte-specific enhancer factor 2, transcript variant X7
myocyte-specific enhancer factor 2, transcript variant X11
myocyte-specific enhancer factor 2, transcript variant X6
myocyte-specific enhancer factor 2, transcript variant X9
myocyte-specific enhancer factor 2, transcript variant X3
myocyte-specific enhancer factor 2, transcript variant X5
myocyte-specific enhancer factor 2, transcript variant X1
myocyte-specific enhancer factor 2, transcript variant X13
myocyte-specific enhancer factor 2 isoform X12
myocyte-specific enhancer factor 2 isoform X14
myocyte-specific enhancer factor 2 isoform X4
myocyte-specific enhancer factor 2 isoform X13
myocyte-specific enhancer factor 2 isoform X10
myocyte-specific enhancer factor 2 isoform X8
myocyte-specific enhancer factor 2 isoform X2
myocyte-specific enhancer factor 2 isoform X7
myocyte-specific enhancer factor 2 isoform X11
myocyte-specific enhancer factor 2 isoform X6
myocyte-specific enhancer factor 2 isoform X9
myocyte-specific enhancer factor 2 isoform X3
myocyte-specific enhancer factor 2 isoform X5
myocyte-specific enhancer factor 2 isoform X1
transfer RNA histidin (anticodon GUG); 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: 9 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
peptidylglycine alpha-hydroxylating monooxygenase
transfer RNA valine (anticodon AAC); 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: 5 Proteins
tyrosine-protein kinase Dnt, transcript variant X2
tyrosine-protein kinase Dnt, transcript variant X1
transfer RNA serine (anticodon CGA); 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: 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription factor Ken, transcript variant X3
transcription factor Ken, transcript variant X2
transcription factor Ken, transcript variant X1
protein bunched, class 2/F/G isoform-like, transcript variant X3
protein bunched, class 2/F/G isoform-like, transcript variant X1
protein bunched, class 2/F/G isoform-like, transcript variant X2
protein bunched, class 2/F/G isoform-like isoform X1
protein bunched, class 2/F/G isoform-like isoform X2
protein bunched, class 2/F/G isoform-like isoform X3
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
conserved oligomeric Golgi complex subunit 3, transcript variant X2
conserved oligomeric Golgi complex subunit 3, transcript variant X1
conserved oligomeric Golgi complex subunit 3
mitochondrial-processing peptidase subunit beta
mitochondrial folate transporter/carrier, transcript variant X1
mitochondrial folate transporter/carrier, transcript variant X2
mitochondrial folate transporter/carrier, transcript variant X3
mitochondrial folate transporter/carrier isoform X1
mitochondrial folate transporter/carrier isoform X2
ras-related protein Rab-32, transcript variant X2
ras-related protein Rab-32, transcript variant X3
ras-related protein Rab-32, transcript variant X5
ras-related protein Rab-32, transcript variant X1
EF-hand calcium-binding domain-containing protein 4B isoform X1
ras-related protein Rab-32, transcript variant X4
ras-related protein Rab-32, transcript variant X7
ras-related protein Rab-32, transcript variant X6
protein brown-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein brown-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein brown-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 1 sample with support for all annotated introns
protein scarlet-like, transcript variant X1
protein scarlet-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 8 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: 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: 97% coverage of the annotated genomic feature by RNAseq alignments
probable peroxisomal acyl-coenzyme A oxidase 1
probable peroxisomal acyl-coenzyme A oxidase 1, transcript variant X2
probable peroxisomal acyl-coenzyme A oxidase 1, transcript variant X1
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 3 samples with support for all annotated introns
probable peroxisomal acyl-coenzyme A oxidase 1 isoform X1
probable peroxisomal acyl-coenzyme A oxidase 1 isoform 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
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: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
probable peroxisomal acyl-coenzyme A oxidase 1, transcript variant X6
probable peroxisomal acyl-coenzyme A oxidase 1, transcript variant X3
probable peroxisomal acyl-coenzyme A oxidase 1, transcript variant X4
probable peroxisomal acyl-coenzyme A oxidase 1, transcript variant X5
oocyte zinc finger protein XlCOF6.1-like, transcript variant X2
oocyte zinc finger protein XlCOF6.1-like isoform X2
oocyte zinc finger protein XlCOF6.1-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 14 samples with support for all annotated introns
oocyte zinc finger protein XlCOF6.1-like isoform X1
zinc finger protein 32-like, transcript variant X1
zinc finger protein 32-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 8 samples with support for all annotated introns
zinc finger protein 32-like, transcript variant X3
N-acetylgalactosamine kinase, 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
N-acetylgalactosamine kinase, 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
translation initiation factor eIF-2B subunit delta, transcript variant X1
translation initiation factor eIF-2B subunit delta, transcript variant X2
translation initiation factor eIF-2B subunit delta isoform X1
translation initiation factor eIF-2B subunit delta isoform X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1
solute carrier organic anion transporter family member 74D, transcript variant X2
solute carrier organic anion transporter family member 74D, transcript variant X4
solute carrier organic anion transporter family member 74D, transcript variant X1
solute carrier organic anion transporter family member 74D, transcript variant X3
solute carrier organic anion transporter family member 74D isoform X1
solute carrier organic anion transporter family member 74D isoform X2
glycine-rich cell wall structural protein-like
glycine-rich cell wall structural protein-like, transcript variant X2
glycine-rich cell wall structural protein-like, transcript variant X3
glycine-rich cell wall structural protein-like, transcript variant X1
glycine-rich cell wall structural protein-like isoform X3
glycine-rich cell wall structural protein-like isoform X2
glycine-rich cell wall structural protein-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% 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, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glycine-rich cell wall structural protein 1.8-like, transcript variant X3
glycine-rich cell wall structural protein 1.8-like, transcript variant X2
glycine-rich cell wall structural protein 1.8-like, transcript variant X1
glycine-rich cell wall structural protein 1.8-like isoform X2
keratin, type II cytoskeletal 3-like, transcript variant X1
keratin, type II cytoskeletal 3-like, transcript variant X2
keratin, type II cytoskeletal 3-like isoform X2
glycine-rich cell wall structural protein 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
BLOC-1-related complex subunit 8 homolog
epidermal retinol dehydrogenase 2-like, transcript variant X5
epidermal retinol dehydrogenase 2-like, transcript variant X3
epidermal retinol dehydrogenase 2-like, transcript variant X1
epidermal retinol dehydrogenase 2-like, transcript variant X4
epidermal retinol dehydrogenase 2-like isoform X1
epidermal retinol dehydrogenase 2-like, transcript variant X2
epidermal retinol dehydrogenase 2-like isoform X2
epidermal retinol dehydrogenase 2-like isoform X3
protein lin-10-like, transcript variant X5
protein lin-10-like, transcript variant X6
protein lin-10-like, transcript variant X7
protein lin-10-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein lin-10-like, transcript variant X1
protein lin-10-like, transcript variant X3
protein lin-10-like, transcript variant X4
uncharacterized protein LOC123876409 isoform X1
uncharacterized protein LOC123876409 isoform X2
amyloid-beta A4 precursor protein-binding family A member 2-like isoform X3
calcium and integrin-binding family member 3
uncharacterized LOC123871169, transcript variant X2
uncharacterized LOC123871169, transcript variant X3
uncharacterized protein LOC123871169 isoform X2
uncharacterized protein LOC123871169 isoform X3
uncharacterized LOC123871169, transcript variant X1
uncharacterized protein LOC123871169 isoform X1
galanin receptor type 3, transcript variant X1
galanin receptor type 3, transcript variant X2
pre-rRNA-processing protein esf2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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 11 samples with support for all annotated introns
pre-rRNA-processing protein esf2-like, transcript variant X1
G1/S-specific cyclin-E, 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 2 samples with support for all annotated introns
G1/S-specific cyclin-E, 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 2 samples with support for all annotated introns
G1/S-specific cyclin-E, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
structural maintenance of chromosomes protein 6
alpha-endosulfine, 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 6 samples with support for all annotated introns
alpha-endosulfine, transcript variant X1
uncharacterized LOC123874624, 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
uncharacterized LOC123874624, transcript variant X2
ribonucleoside-diphosphate reductase subunit M2, transcript variant X2
COP9 signalosome complex subunit 2, transcript variant X2
COP9 signalosome complex subunit 2, transcript variant X1
COP9 signalosome complex subunit 2 isoform X2
COP9 signalosome complex subunit 2 isoform X1
ribonucleoside-diphosphate reductase subunit M2, transcript variant X1
ribonucleoside-diphosphate reductase subunit M2
neuroblastoma-amplified sequence-like, transcript variant X1
neuroblastoma-amplified sequence-like, transcript variant X2
neuroblastoma-amplified sequence-like isoform X1
neuroblastoma-amplified sequence-like isoform X2
28S ribosomal protein S11, mitochondrial
coiled-coil domain-containing protein 124, transcript variant X1
coiled-coil domain-containing protein 124, transcript variant X2
coiled-coil domain-containing protein 124, transcript variant X3
coiled-coil domain-containing protein 124
2-(3-amino-3-carboxypropyl)histidine synthase subunit 2
14 kDa phosphohistidine phosphatase-like
putative uncharacterized protein DDB_G0291608
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
toll-like receptor 4, transcript variant X2
toll-like receptor 4, 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 27 samples with support for all annotated introns
rho GTPase-activating protein conundrum, transcript variant X1
rho GTPase-activating protein conundrum isoform X1
rho GTPase-activating protein conundrum, transcript variant X2
rho GTPase-activating protein conundrum isoform X2
rho GTPase-activating protein conundrum, 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 7 samples with support for all annotated introns
rho GTPase-activating protein conundrum isoform X3
uncharacterized LOC123874672, transcript variant X2
uncharacterized LOC123874672, transcript variant X1
uncharacterized LOC123874672, transcript variant X4
uncharacterized LOC123874672, transcript variant X6
uncharacterized LOC123874672, transcript variant X3
uncharacterized LOC123874672, transcript variant X5
uncharacterized protein LOC123874672 isoform X2
uncharacterized protein LOC123874672 isoform X1
uncharacterized protein LOC123874672 isoform X3
uncharacterized LOC123874672, transcript variant X8
uncharacterized LOC123874672, transcript variant X7
uncharacterized protein LOC123874672 isoform X4
uncharacterized protein LOC123874672 isoform X5
uncharacterized LOC123874807, transcript variant X2
uncharacterized LOC123874807, transcript variant X1
proteasome subunit beta type-2-like, transcript variant X1
proteasome subunit beta type-2-like isoform X1
proteasome subunit beta type-2-like, transcript variant X2
proteasome subunit beta type-2-like isoform X2
uncharacterized MFS-type transporter C09D4.1, transcript variant X1
uncharacterized MFS-type transporter C09D4.1, transcript variant X2
uncharacterized MFS-type transporter C09D4.1 isoform X1
uncharacterized LOC123871293, transcript variant X2
uncharacterized MFS-type transporter C09D4.1, transcript variant X3
uncharacterized MFS-type transporter C09D4.1 isoform X2
uncharacterized MFS-type transporter C09D4.1, transcript variant X4
uncharacterized MFS-type transporter C09D4.1 isoform X3
uncharacterized LOC123871293, transcript variant X1
NEDD8-conjugating enzyme UBE2F-like, transcript variant X2
NEDD8-conjugating enzyme UBE2F-like, transcript variant X1
vacuolar protein-sorting-associated protein 25-like, transcript variant X2
vacuolar protein-sorting-associated protein 25-like isoform X2
vacuolar protein-sorting-associated protein 25-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 24 samples with support for all annotated introns
inositol-pentakisphosphate 2-kinase-like isoform X1
solute carrier organic anion transporter family member 4A1, 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 2 samples with support for all annotated introns
solute carrier organic anion transporter family member 4A1, transcript variant X2
solute carrier organic anion transporter family member 4A1 isoform X1
solute carrier organic anion transporter family member 4A1 isoform X2
dynein assembly factor with WDR repeat domains 1
dnaJ protein homolog 1, transcript variant X1
dnaJ protein homolog 1, 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 3 samples with support for all annotated introns
ubiquitin-like modifier-activating enzyme 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ubiquitin-like modifier-activating enzyme 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin-like modifier-activating enzyme 5
mutS protein homolog 5-like, transcript variant X2
mutS protein homolog 5-like, transcript variant X3
mutS protein homolog 5-like, transcript variant X1
nucleolar protein dao-5-like, transcript variant X1
nucleolar protein dao-5-like, transcript variant X3
nucleolar protein dao-5-like, transcript variant X2
bromodomain-containing protein 7-like, transcript variant X1
bromodomain-containing protein 7-like, transcript variant X2
bromodomain-containing protein 7-like isoform X1
bromodomain-containing protein 7-like isoform X2
hairy/enhancer-of-split related with YRPW motif protein
serine/threonine-protein kinase 3, transcript variant X6
serine/threonine-protein kinase 3, transcript variant X2
serine/threonine-protein kinase 3, transcript variant X5
serine/threonine-protein kinase 3, transcript variant X4
serine/threonine-protein kinase 3, transcript variant X3
serine/threonine-protein kinase 3, transcript variant X1
serine/threonine-protein kinase 3 isoform X3
serine/threonine-protein kinase 4 isoform X1
serine/threonine-protein kinase 3 isoform X2
cilia- and flagella-associated protein 20
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
leucine carboxyl methyltransferase 1, transcript variant X1
leucine carboxyl methyltransferase 1, transcript variant X2
leucine carboxyl methyltransferase 1 isoform X2
leucine carboxyl methyltransferase 1 isoform X1
probable malonyl-CoA-acyl carrier protein transacylase, mitochondrial
very long-chain specific acyl-CoA dehydrogenase, mitochondrial, transcript variant X1
very long-chain specific acyl-CoA dehydrogenase, mitochondrial, transcript variant X2
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X2
very long-chain specific acyl-CoA dehydrogenase, mitochondrial isoform X1
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 3 samples with support for all annotated introns
zinc finger protein 706-like, transcript variant X1
zinc finger protein 706-like, transcript variant X2
DNA repair protein complementing XP-A cells homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns