Pieris rapae chromosome 2, ilPieRapa1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Papilionoidea; Pieridae; Pierinae; Pieris.
REFSEQ INFORMATION: The reference sequence is identical to\nLR990584.1.\nAssembly name: ilPieRapa1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Wellcome Sanger Institute on\n2021/01/28. The original whole-genome shotgun project has the\naccession CAJHWY000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Pieris rapae Annotation Release 101\nAnnotation Version :: 101\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.
acetylcholine receptor subunit alpha-like
COORDINATES: polyA evidence [ECO:0006239]
NKAP family protein CG6066, transcript variant X2
NKAP family protein CG6066, transcript variant X1
poly [ADP-ribose] polymerase tankyrase, 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 10 samples with support for all annotated introns
poly [ADP-ribose] polymerase tankyrase, 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 2 samples with support for all annotated introns
poly [ADP-ribose] polymerase tankyrase, 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 17 samples with support for all annotated introns
poly [ADP-ribose] polymerase tankyrase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
poly [ADP-ribose] polymerase tankyrase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
poly [ADP-ribose] polymerase tankyrase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
poly [ADP-ribose] polymerase tankyrase isoform X2
coiled-coil domain-containing protein 63-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 1, transcript variant X3
zinc finger protein 1, transcript variant X2
zinc finger protein 1, transcript variant X1
zinc finger protein 1, transcript variant X5
zinc finger protein 1, 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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon AAC); 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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
cytoplasmic dynein 1 intermediate chain, 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 21 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X1
cytoplasmic dynein 1 intermediate chain, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, 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 2 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X7
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 39 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, 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 26 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X11
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 71 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X14
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 21 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain, transcript variant X13
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 37 samples with support for all annotated introns
cytoplasmic dynein 1 intermediate chain isoform X1
cytoplasmic dynein 1 intermediate chain isoform X4
cytoplasmic dynein 1 intermediate chain isoform X5
cytoplasmic dynein 1 intermediate chain isoform X10
cytoplasmic dynein 1 intermediate chain isoform X2
cytoplasmic dynein 1 intermediate chain isoform X7
cytoplasmic dynein 1 intermediate chain isoform X3
cytoplasmic dynein 1 intermediate chain isoform X8
cytoplasmic dynein 1 intermediate chain isoform X9
cytoplasmic dynein 1 intermediate chain isoform X12
cytoplasmic dynein 1 intermediate chain isoform X6
cytoplasmic dynein 1 intermediate chain isoform X11
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial, transcript variant X3
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial, transcript variant X1
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial, transcript variant X2
3-hydroxyisobutyryl-CoA hydrolase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 431, 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 42 samples with support for all annotated introns
zinc finger protein 431, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
zinc finger protein 431, transcript variant X2
protein odd-skipped-related 2 isoform X2
moesin/ezrin/radixin homolog 1, transcript variant X3
moesin/ezrin/radixin homolog 1, transcript variant X1
moesin/ezrin/radixin homolog 1, transcript variant X2
moesin/ezrin/radixin homolog 1 isoform X3
moesin/ezrin/radixin homolog 1 isoform X2
moesin/ezrin/radixin homolog 1 isoform X1
phospholipase B1, membrane-associated-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
V-type proton ATPase 116 kDa subunit a1, transcript variant X2
V-type proton ATPase 116 kDa subunit a1, transcript variant X1
V-type proton ATPase 116 kDa subunit a1, transcript variant X4
V-type proton ATPase 116 kDa subunit a1, transcript variant X3
V-type proton ATPase 116 kDa subunit a1 isoform X2
V-type proton ATPase 116 kDa subunit a1 isoform X1
V-type proton ATPase 116 kDa subunit a1 isoform X4
V-type proton ATPase 116 kDa subunit a1 isoform X3
uncharacterized LOC111004075, transcript variant X2
uncharacterized LOC111004075, transcript variant X1
uncharacterized protein LOC111004075 isoform X2
uncharacterized protein LOC111004075 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
von Willebrand factor D and EGF domain-containing protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
cell wall protein DAN4, 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 32 samples with support for all annotated introns
cell wall protein DAN4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
cell wall protein DAN4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC111004091, transcript variant X1
uncharacterized protein LOC111004091 isoform X1
uncharacterized LOC111004091, 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 19 samples with support for all annotated introns
uncharacterized protein LOC111004091 isoform X2
U3 small nucleolar RNA-associated protein 18 homolog
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic, transcript variant X1
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic, transcript variant X4
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic, transcript variant X2
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic, transcript variant X3
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic isoform X4
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic isoform X1
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic isoform X2
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic isoform X3
methionyl-tRNA formyltransferase, mitochondrial
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 9 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 2 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 186 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like isoform X1
acetylcholine receptor subunit alpha-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acetylcholine receptor subunit alpha-like 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 6 samples with support for all annotated introns
uncharacterized LOC123689861, transcript variant X2
uncharacterized LOC123689861, transcript variant X1
beta-1,4-mannosyltransferase egh, 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 26 samples with support for all annotated introns
beta-1,4-mannosyltransferase egh, 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
beta-1,4-mannosyltransferase egh isoform X1
beta-1,4-mannosyltransferase egh isoform X2
disintegrin and metalloproteinase domain-containing protein 10
peptidyl-prolyl cis-trans isomerase F, 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 4 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
proton-associated sugar transporter A, transcript variant X1
proton-associated sugar transporter A, transcript variant X2
thiamin pyrophosphokinase 1, transcript variant X3
thiamin pyrophosphokinase 1, transcript variant X1
thiamin pyrophosphokinase 1, transcript variant X2
tetratricopeptide repeat protein 21B, 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 20 samples with support for all annotated introns
tetratricopeptide repeat protein 21B, transcript variant X2
uncharacterized LOC110995596, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC110995596, transcript variant X9
uncharacterized LOC110995596, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC110995596, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC110995596, transcript variant X1
uncharacterized LOC110995596, transcript variant X6
uncharacterized LOC110995596, transcript variant X4
uncharacterized LOC110995596, transcript variant X5
uncharacterized LOC110995596, transcript variant X2
uncharacterized LOC110995596, transcript variant X3
uncharacterized protein LOC110995596 isoform X1
uncharacterized protein LOC110995596 isoform X4
uncharacterized protein LOC110995596 isoform X2
uncharacterized protein LOC110995596 isoform X3
uncharacterized protein LOC110995596 isoform X7
uncharacterized protein LOC110995596 isoform X8
uncharacterized protein LOC110995596 isoform X9
uncharacterized protein LOC110995596 isoform X6
uncharacterized LOC110995596, transcript variant X7
uncharacterized protein LOC110995596 isoform X5
uncharacterized LOC110995611, transcript variant X1
uncharacterized LOC110995611, 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 12 samples with support for all annotated introns
uncharacterized protein LOC110995611 isoform X2
uncharacterized protein LOC110995611 isoform X1
acyl-CoA Delta(11) desaturase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-CoA Delta(11) desaturase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
acyl-CoA Delta(11) desaturase isoform X1
acyl-CoA Delta(11) desaturase isoform X2
acyl-CoA Delta(11) desaturase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-CoA Delta(11) desaturase-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 32 samples with support for all annotated introns
uncharacterized protein C15orf61 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NPC intracellular cholesterol transporter 1
bifunctional purine biosynthesis protein ATIC
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 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 105 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich melanocyte differentiation-associated 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 24 samples with support for all annotated introns
SH3 domain-containing kinase-binding protein 1, transcript variant X1
SH3 domain-containing kinase-binding protein 1, transcript variant X3
SH3 domain-containing kinase-binding protein 1, transcript variant X4
SH3 domain-containing kinase-binding protein 1, transcript variant X2
SH3 domain-containing kinase-binding protein 1 isoform X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 2, mitochondrial-like
uncharacterized LOC110995193, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC110995193, 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 3 samples with support for all annotated introns
uncharacterized protein LOC110995193 isoform X1
uncharacterized protein LOC110995193 isoform X2
uncharacterized LOC110995186, 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 6 samples with support for all annotated introns
uncharacterized protein LOC110995186 isoform X1
uncharacterized LOC110995186, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized protein LOC110995186 isoform X3
uncharacterized LOC110995186, 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 13 samples with support for all annotated introns
uncharacterized LOC110995186, 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 14 samples with support for all annotated introns
uncharacterized protein LOC110995186 isoform X2
mannosyl-oligosaccharide alpha-1,2-mannosidase IA, transcript variant X1
mannosyl-oligosaccharide alpha-1,2-mannosidase IA isoform X1
mannosyl-oligosaccharide alpha-1,2-mannosidase IA, transcript variant X2
mannosyl-oligosaccharide alpha-1,2-mannosidase IA isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC110995190, transcript variant X1
uncharacterized LOC110995190, transcript variant X2
CDGSH iron-sulfur domain-containing protein 2 homolog
PH and SEC7 domain-containing protein, transcript variant X1
PH and SEC7 domain-containing protein, transcript variant X2
PH and SEC7 domain-containing protein isoform X1
PH and SEC7 domain-containing protein isoform X2
PH and SEC7 domain-containing protein, transcript variant X3
PH and SEC7 domain-containing protein isoform X3
tubby-related protein 4, transcript variant X2
tubby-related protein 4, transcript variant X1
tubby-related protein 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DNA polymerase theta, 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 7 samples with support for all annotated introns
DNA polymerase theta, 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 14 samples with support for all annotated introns
UPF0415 protein C7orf25 homolog, transcript variant X1
UPF0415 protein C7orf25 homolog, 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 7 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 16 samples with support for all annotated introns
interleukin-1 receptor-associated kinase 4
DNA polymerase zeta catalytic subunit, 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 7 samples with support for all annotated introns
DNA polymerase zeta catalytic subunit, 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 16 samples with support for all annotated introns
DNA polymerase zeta catalytic subunit isoform X2
DNA polymerase zeta catalytic subunit 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
disintegrin and metalloproteinase domain-containing protein 10, transcript variant X2
disintegrin and metalloproteinase domain-containing protein 10, 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 14 samples with support for all annotated introns
uncharacterized protein LOC110995185 isoform X1
disintegrin and metalloproteinase domain-containing protein 10 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC110995194, transcript variant X3
uncharacterized LOC110995194, transcript variant X1
uncharacterized LOC110995194, 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
putative thiosulfate sulfurtransferase, mitochondrial
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 3, transcript variant X4
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 3, transcript variant X1
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 3, transcript variant X3
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 3, transcript variant X2
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 3 isoform X1
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 3 isoform X2
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 3 isoform X3
histone-lysine N-methyltransferase 2C, transcript variant X1
histone-lysine N-methyltransferase 2C, transcript variant X3
histone-lysine N-methyltransferase 2C, transcript variant X8
histone-lysine N-methyltransferase 2C, transcript variant X9
histone-lysine N-methyltransferase 2C, transcript variant X11
histone-lysine N-methyltransferase 2C, transcript variant X2
histone-lysine N-methyltransferase 2C, transcript variant X7
histone-lysine N-methyltransferase 2C, transcript variant X10
histone-lysine N-methyltransferase 2C, transcript variant X6
histone-lysine N-methyltransferase 2C, transcript variant X5
histone-lysine N-methyltransferase 2C, transcript variant X12
histone-lysine N-methyltransferase 2C, transcript variant X4
histone-lysine N-methyltransferase 2C isoform X1
histone-lysine N-methyltransferase 2C isoform X3
histone-lysine N-methyltransferase 2C isoform X8
histone-lysine N-methyltransferase 2C isoform X9
histone-lysine N-methyltransferase 2C isoform X11
histone-lysine N-methyltransferase 2C isoform X2
histone-lysine N-methyltransferase 2C isoform X7
histone-lysine N-methyltransferase 2C isoform X10
histone-lysine N-methyltransferase 2C isoform X6
histone-lysine N-methyltransferase 2C isoform X5
histone-lysine N-methyltransferase 2C isoform X12
histone-lysine N-methyltransferase 2C isoform X4
GTP-binding protein SAR1b, transcript variant X1
GTP-binding protein SAR1b, transcript variant X2
cytosolic carboxypeptidase-like protein 5, transcript variant X1
cytosolic carboxypeptidase-like protein 5, transcript variant X2
cytosolic carboxypeptidase-like protein 5, transcript variant X3
cytosolic carboxypeptidase-like protein 5, transcript variant X5
cytosolic carboxypeptidase-like protein 5, transcript variant X6
cytosolic carboxypeptidase-like protein 5, transcript variant X4
cytosolic carboxypeptidase-like protein 5 isoform X3
cytosolic carboxypeptidase-like protein 5 isoform X4
cytosolic carboxypeptidase-like protein 5 isoform X2
cytosolic carboxypeptidase-like protein 5 isoform X1
uncharacterized LOC110995163, transcript variant X1
uncharacterized LOC110995163, transcript variant X2
uncharacterized protein LOC110995163 isoform X1
uncharacterized protein LOC110995163 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 9 samples with support for all annotated introns
tachykinin-like peptides receptor 99D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tachykinin-like peptides receptor 99D, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tachykinin-like peptides receptor 99D, transcript variant X3
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 4 samples with support for all annotated introns
tachykinin-like peptides receptor 99D isoform X2
tachykinin-like peptides receptor 99D isoform X3
tachykinin-like peptides receptor 99D isoform X1
probable ubiquitin carboxyl-terminal hydrolase 9, transcript variant X1
probable ubiquitin carboxyl-terminal hydrolase 9, transcript variant X2
probable ubiquitin carboxyl-terminal hydrolase 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
geranylgeranyl pyrophosphate synthase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 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 56 samples with support for all annotated introns
calcium-activated potassium channel slowpoke, transcript variant X12
calcium-activated potassium channel slowpoke, transcript variant X13
calcium-activated potassium channel slowpoke, transcript variant X10
calcium-activated potassium channel slowpoke, transcript variant X5
calcium-activated potassium channel slowpoke, transcript variant X4
calcium-activated potassium channel slowpoke, transcript variant X7
calcium-activated potassium channel slowpoke, transcript variant X2
calcium-activated potassium channel slowpoke, transcript variant X3
calcium-activated potassium channel slowpoke, transcript variant X6
calcium-activated potassium channel slowpoke, transcript variant X14
calcium-activated potassium channel slowpoke, transcript variant X8
calcium-activated potassium channel slowpoke, transcript variant X1
calcium-activated potassium channel slowpoke, transcript variant X19
calcium-activated potassium channel slowpoke, transcript variant X17
calcium-activated potassium channel slowpoke, transcript variant X11
calcium-activated potassium channel slowpoke, transcript variant X16
calcium-activated potassium channel slowpoke, transcript variant X18
calcium-activated potassium channel slowpoke, transcript variant X15
calcium-activated potassium channel slowpoke, transcript variant X9
calcium-activated potassium channel slowpoke isoform X7
calcium-activated potassium channel slowpoke isoform X2
calcium-activated potassium channel slowpoke isoform X12
calcium-activated potassium channel slowpoke isoform X3
calcium-activated potassium channel slowpoke isoform X13
calcium-activated potassium channel slowpoke isoform X10
calcium-activated potassium channel slowpoke isoform X19
calcium-activated potassium channel slowpoke isoform X17
calcium-activated potassium channel slowpoke isoform X11
calcium-activated potassium channel slowpoke isoform X16
calcium-activated potassium channel slowpoke isoform X6
calcium-activated potassium channel slowpoke isoform X18
calcium-activated potassium channel slowpoke isoform X15
calcium-activated potassium channel slowpoke isoform X14
calcium-activated potassium channel slowpoke isoform X8
calcium-activated potassium channel slowpoke isoform X9
calcium-activated potassium channel slowpoke isoform X1
calcium-activated potassium channel slowpoke isoform X5
calcium-activated potassium channel slowpoke isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC110995333, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC110995333, 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 9 samples with support for all annotated introns
uncharacterized protein LOC110995333 isoform X2
uncharacterized protein LOC110995333 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
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 112 samples with support for all annotated introns
calcium-binding mitochondrial carrier protein Aralar1, transcript variant X3
calcium-binding mitochondrial carrier protein Aralar1, transcript variant X2
calcium-binding mitochondrial carrier protein Aralar1, transcript variant X1
calcium-binding mitochondrial carrier protein Aralar1, transcript variant X6
calcium-binding mitochondrial carrier protein Aralar1, transcript variant X5
calcium-binding mitochondrial carrier protein Aralar1, transcript variant X4
calcium-binding mitochondrial carrier protein Aralar1 isoform X3
calcium-binding mitochondrial carrier protein Aralar1 isoform X1
calcium-binding mitochondrial carrier protein Aralar1 isoform X2
calcium-binding mitochondrial carrier protein Aralar1 isoform X4
oxamate amidohydrolase proenzyme, transcript variant X2
oxamate amidohydrolase proenzyme, transcript variant X1
acid sphingomyelinase-like phosphodiesterase 3a
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: 16 Proteins
uncharacterized LOC110995335, transcript variant X5
uncharacterized LOC110995335, transcript variant X4
uncharacterized LOC110995335, transcript variant X3
uncharacterized LOC110995335, transcript variant X1
uncharacterized LOC110995335, transcript variant X2
uncharacterized protein LOC110995335 isoform X4
uncharacterized protein LOC110995335 isoform X3
uncharacterized protein LOC110995335 isoform X2
uncharacterized protein LOC110995335 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC110998845, transcript variant X3
uncharacterized LOC110998845, transcript variant X2
uncharacterized protein LOC110998845 isoform X2
uncharacterized protein LOC110998845 isoform X3
uncharacterized LOC110998845, transcript variant X5
uncharacterized LOC110998845, transcript variant X4
uncharacterized LOC110998845, transcript variant X1
uncharacterized protein LOC110998845 isoform X1
alkylglycerol monooxygenase, transcript variant X1
alkylglycerol monooxygenase, 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
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
centaurin-gamma-1A, transcript variant X1
centaurin-gamma-1A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
angiotensin-converting enzyme, transcript variant X1
angiotensin-converting enzyme, transcript variant X2
angiotensin-converting enzyme isoform X1
angiotensin-converting enzyme isoform X2
angiotensin-converting enzyme, transcript variant X3
angiotensin-converting enzyme isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
proline-rich protein 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
proline-rich protein 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
juvenile hormone esterase-like, transcript variant X3
juvenile hormone esterase-like, transcript variant X5
juvenile hormone esterase-like, transcript variant X2
juvenile hormone esterase-like, transcript variant X1
juvenile hormone esterase-like isoform X1
juvenile hormone esterase-like, transcript variant X4
juvenile hormone esterase-like isoform X2
uncharacterized LOC123690168, transcript variant X2
uncharacterized LOC123690168, transcript variant X1
importin subunit alpha-7, transcript variant X2
importin subunit alpha-7, transcript variant X1
ATP synthase subunit beta, mitochondrial-like
ubiquinol-cytochrome-c reductase complex assembly factor 1
ATP synthase subunit beta, mitochondrial
uncharacterized LOC110996481, transcript variant X2
uncharacterized LOC110996481, transcript variant X1
NEDD8-activating enzyme E1 catalytic subunit
signal peptidase complex catalytic subunit SEC11A
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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
serine protease nudel, transcript variant X2
serine protease nudel, transcript variant X3
serine protease nudel, transcript variant X1
serine protease nudel, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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
corticotropin-releasing factor-binding protein
protein bric-a-brac 1, transcript variant X5
protein bric-a-brac 1, transcript variant X2
protein bric-a-brac 1, transcript variant X3
protein bric-a-brac 1, transcript variant X4
protein bric-a-brac 1, transcript variant X1
protein bric-a-brac 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 45 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 77 samples with support for all annotated introns
S-adenosylmethionine synthase, transcript variant X1
S-adenosylmethionine synthase, transcript variant X2
S-adenosylmethionine synthase, transcript variant X3
S-adenosylmethionine synthase isoform X1
S-adenosylmethionine synthase isoform X2
PHD finger protein 14, transcript variant X1
PHD finger protein 14, transcript variant X6
PHD finger protein 14, transcript variant X4
PHD finger protein 14, transcript variant X2
PHD finger protein 14, transcript variant X7
PHD finger protein 14, transcript variant X3
PHD finger protein 14, 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
arylsulfatase I-like, transcript variant X1
arylsulfatase I-like, transcript variant X3
arylsulfatase I-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
arylsulfatase B-like, transcript variant X2
arylsulfatase B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
transcription initiation factor TFIID subunit 13, transcript variant X2
transcription initiation factor TFIID subunit 13, transcript variant X4
transcription initiation factor TFIID subunit 13, transcript variant X6
transcription initiation factor TFIID subunit 13, transcript variant X1
transcription initiation factor TFIID subunit 13, transcript variant X3
transcription initiation factor TFIID subunit 13, transcript variant X5
transcription initiation factor TFIID subunit 13, transcript variant X8
transcription initiation factor TFIID subunit 13, transcript variant X10
transcription initiation factor TFIID subunit 13, transcript variant X12
transcription initiation factor TFIID subunit 13, transcript variant X7
transcription initiation factor TFIID subunit 13, transcript variant X9
transcription initiation factor TFIID subunit 13, transcript variant X11
transcription initiation factor TFIID subunit 13, transcript variant X14
transcription initiation factor TFIID subunit 13, transcript variant X15
transcription initiation factor TFIID subunit 13, transcript variant X16
transcription initiation factor TFIID subunit 13, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 117 samples with support for all annotated introns
transcription initiation factor TFIID subunit 13 isoform X4
transcription initiation factor TFIID subunit 13 isoform X1
transcription initiation factor TFIID subunit 13 isoform X2
transcription initiation factor TFIID subunit 13 isoform X3
uncharacterized LOC110996434, 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
uncharacterized LOC110996434, 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 11 samples with support for all annotated introns
uncharacterized LOC110996434, transcript variant X3
uncharacterized protein LOC110996434 isoform X3
uncharacterized protein LOC110996434 isoform X2
uncharacterized protein LOC110996434 isoform X1
uncharacterized LOC110996435, 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 11 samples with support for all annotated introns
uncharacterized protein LOC110996435 isoform X1
uncharacterized LOC110996435, 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 39 samples with support for all annotated introns
uncharacterized protein LOC110996435 isoform X2
glutamate-gated chloride channel, transcript variant X15
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
glutamate-gated chloride channel, transcript variant X13
glutamate-gated chloride channel, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glutamate-gated chloride channel, 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 1 sample with support for all annotated introns
glutamate-gated chloride channel, transcript variant X19
glutamate-gated chloride channel, transcript variant X18
glutamate-gated chloride channel, transcript variant X17
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
glutamate-gated chloride channel, transcript variant X12
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
glutamate-gated chloride channel, 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 3 samples with support for all annotated introns
glutamate-gated chloride channel, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glutamate-gated chloride channel, transcript variant X6
glutamate-gated chloride channel, transcript variant X5
glutamate-gated chloride channel, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate-gated chloride channel, transcript variant X2
glutamate-gated chloride channel, transcript variant X1
glutamate-gated chloride channel, transcript variant X14
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
glutamate-gated chloride channel, transcript variant X16
glutamate-gated chloride channel, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glutamate-gated chloride channel, transcript variant X8
glutamate-gated chloride channel isoform X14
glutamate-gated chloride channel isoform X15
glutamate-gated chloride channel isoform X13
glutamate-gated chloride channel isoform X10
glutamate-gated chloride channel subunit beta isoform X7
glutamate-gated chloride channel subunit beta isoform X19
glutamate-gated chloride channel alpha isoform X18
glutamate-gated chloride channel subunit beta isoform X16
glutamate-gated chloride channel isoform X11
glutamate-gated chloride channel isoform X8
glutamate-gated chloride channel isoform X17
glutamate-gated chloride channel isoform X12
glutamate-gated chloride channel isoform X9
glutamate-gated chloride channel isoform X4
glutamate-gated chloride channel subunit beta isoform X6
glycine receptor subunit alpha-4 isoform X5
glycine receptor subunit alpha-3 isoform X3
glutamate-gated chloride channel subunit beta isoform X2
glutamate-gated chloride channel subunit beta isoform X1
poly(rC)-binding protein 3, transcript variant X6
poly(rC)-binding protein 3, transcript variant X7
poly(rC)-binding protein 3, transcript variant X2
poly(rC)-binding protein 3, transcript variant X1
poly(rC)-binding protein 3, transcript variant X4
poly(rC)-binding protein 3, transcript variant X5
poly(rC)-binding protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins
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
molybdenum cofactor sulfurase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
molybdenum cofactor sulfurase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ras-related protein Rab-27A, transcript variant X1
ras-related protein Rab-27A, transcript variant X2
sorbin and SH3 domain-containing protein 1, transcript variant X8
sorbin and SH3 domain-containing protein 1, transcript variant X10
sorbin and SH3 domain-containing protein 1, transcript variant X9
sorbin and SH3 domain-containing protein 1, transcript variant X12
sorbin and SH3 domain-containing protein 1 isoform X8
sorbin and SH3 domain-containing protein 1 isoform X12
sorbin and SH3 domain-containing protein 1 isoform X10
sorbin and SH3 domain-containing protein 1 isoform X9
sorbin and SH3 domain-containing protein 1, transcript variant X11
sorbin and SH3 domain-containing protein 1 isoform X11
sorbin and SH3 domain-containing protein 1, transcript variant X13
sorbin and SH3 domain-containing protein 1, transcript variant X1
sorbin and SH3 domain-containing protein 1, transcript variant X4
sorbin and SH3 domain-containing protein 1, transcript variant X5
sorbin and SH3 domain-containing protein 1, transcript variant X6
sorbin and SH3 domain-containing protein 1, transcript variant X7
sorbin and SH3 domain-containing protein 1, transcript variant X2
sorbin and SH3 domain-containing protein 1, transcript variant X3
uncharacterized protein LOC110996449 isoform X13
uncharacterized protein LOC110996449 isoform X1
uncharacterized protein LOC110996449 isoform X4
uncharacterized protein LOC110996449 isoform X5
uncharacterized protein LOC110996449 isoform X6
uncharacterized protein LOC110996449 isoform X7
uncharacterized protein LOC110996449 isoform X2
uncharacterized protein LOC110996449 isoform X3
putative sodium-dependent multivitamin transporter, transcript variant X1
putative sodium-dependent multivitamin transporter, transcript variant X2
putative sodium-dependent multivitamin transporter
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
putative sodium-dependent multivitamin transporter, transcript variant X3
putative sodium-dependent multivitamin transporter, transcript variant X5
putative sodium-dependent multivitamin transporter, transcript variant X4
putative sodium-dependent multivitamin transporter isoform X1
putative sodium-dependent multivitamin transporter isoform X2
putative sodium-dependent multivitamin transporter isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC110996473, transcript variant X2
uncharacterized LOC110996473, transcript variant X1
uncharacterized protein LOC110996473 isoform X2
uncharacterized protein LOC110996473 isoform X1
cell division cycle and apoptosis regulator protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
early boundary activity protein 2-like, transcript variant X2
early boundary activity protein 2-like, transcript variant X1
uncharacterized protein LOC110996488 isoform X1
early boundary activity protein 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 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 7 samples with support for all annotated introns
uncharacterized LOC111001001, 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 13 samples with support for all annotated introns
uncharacterized protein LOC111001001 isoform X1
uncharacterized LOC111001001, transcript variant X4
uncharacterized LOC111001001, 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 30 samples with support for all annotated introns
uncharacterized LOC111001001, transcript variant X2
uncharacterized protein LOC111001001 isoform X4
uncharacterized protein LOC111001001 isoform X3
uncharacterized protein LOC111001001 isoform X2
acidic leucine-rich nuclear phosphoprotein 32 family member A, 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 35 samples with support for all annotated introns
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X1
acidic leucine-rich nuclear phosphoprotein 32 family member A, transcript variant X2
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X1
acidic leucine-rich nuclear phosphoprotein 32 family member A isoform X2
origin recognition complex subunit 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
origin recognition complex subunit 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
origin recognition complex subunit 2 isoform X1
origin recognition complex subunit 2 isoform X2
origin recognition complex subunit 2, transcript variant X3
uncharacterized protein LOC111000998 isoform X3
huntingtin-interacting protein K, transcript variant X1
huntingtin-interacting protein K, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 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: 14 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: 11 Proteins, and 32% 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 52% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X3
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X6
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X1
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X5
guanine nucleotide-binding protein G(q) subunit alpha isoform X3
guanine nucleotide-binding protein G(q) subunit alpha isoform X1
guanine nucleotide-binding protein G(q) subunit alpha isoform X5
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X4
guanine nucleotide-binding protein G(q) subunit alpha, transcript variant X2
fatty-acid amide hydrolase 2-B, transcript variant X2
fatty-acid amide hydrolase 2-B, transcript variant X3
fatty-acid amide hydrolase 2-B, transcript variant X1
fatty-acid amide hydrolase 2-B isoform X1
fatty-acid amide hydrolase 2-B isoform X2
zinc finger MIZ domain-containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
zinc finger MIZ domain-containing protein 1, 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 21 samples with support for all annotated introns
zinc finger MIZ domain-containing protein 1
uncharacterized LOC110998189, 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 15 samples with support for all annotated introns
uncharacterized LOC110998189, 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 10 samples with support for all annotated introns
uncharacterized protein LOC110998189 isoform X1
uncharacterized LOC110998189, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC110998189 isoform X2
uncharacterized LOC110998189, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein LOC110998189 isoform 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 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X5
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X4
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X3
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X2
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial, transcript variant X1
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X4
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X3
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X2
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X5
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial isoform X1
polypeptide N-acetylgalactosaminyltransferase 5, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 5, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 5
mitogen-activated protein kinase kinase kinase 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments
putative neuropeptide precursor protein, transcript variant X3
putative neuropeptide precursor protein, transcript variant X1
putative neuropeptide precursor protein, transcript variant X2
putative neuropeptide precursor protein isoform X3
putative neuropeptide precursor protein isoform X2
putative neuropeptide precursor protein isoform X1
peptidyl-prolyl cis-trans isomerase sig-7
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
carboxypeptidase B-like, transcript variant X1
carboxypeptidase B-like, transcript variant X2
runt-related transcription factor 3, transcript variant X2
runt-related transcription factor 3, transcript variant X1
runt-related transcription factor 3 isoform X2
runt-related transcription factor 3 isoform 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 16 samples with support for all annotated introns
pre-mRNA-splicing regulator female-lethal(2)D
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC110998560, transcript variant X2
uncharacterized LOC110998560, transcript variant X1
probable ribonuclease ZC3H12B, transcript variant X1
probable ribonuclease ZC3H12B, transcript variant X4
probable ribonuclease ZC3H12B, transcript variant X2
probable ribonuclease ZC3H12B, transcript variant X3
probable ribonuclease ZC3H12C isoform X1
probable ribonuclease ZC3H12B isoform X4
probable ribonuclease ZC3H12B isoform X3
probable ribonuclease ZC3H12B isoform X2
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X2
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X1
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial, transcript variant X3
NADH-ubiquinone oxidoreductase 75 kDa subunit, mitochondrial
reversion-inducing cysteine-rich protein with Kazal motifs
brefeldin A-inhibited guanine nucleotide-exchange protein 3
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 5, mitochondrial
malate dehydrogenase, transcript variant X3
chromatin assembly factor 1 subunit A-A isoform X3
pancreatic triacylglycerol lipase, transcript variant X4
pancreatic triacylglycerol lipase, transcript variant X3
pancreatic triacylglycerol lipase, transcript variant X1
pancreatic triacylglycerol lipase, transcript variant X5
pancreatic triacylglycerol lipase, transcript variant X2
pancreatic triacylglycerol lipase isoform X1
malate dehydrogenase, transcript variant X4
malate dehydrogenase, transcript variant X1
malate dehydrogenase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon UGA); 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
probable ATP-dependent RNA helicase DDX46, transcript variant X1
probable ATP-dependent RNA helicase DDX46
probable ATP-dependent RNA helicase DDX46, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
U6 snRNA-associated Sm-like protein LSm3
U3 small nucleolar RNA-associated protein 14 homolog A
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 54 samples with support for all annotated introns
uncharacterized protein DDB_G0287625-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
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial, transcript variant X1
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial, transcript variant X2
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial isoform X1
isocitrate dehydrogenase [NAD] subunit beta, mitochondrial isoform X2
ileal sodium/bile acid cotransporter, transcript variant X4
ileal sodium/bile acid cotransporter, transcript variant X2
ileal sodium/bile acid cotransporter, transcript variant X5
ileal sodium/bile acid cotransporter, transcript variant X3
ileal sodium/bile acid cotransporter, transcript variant X1
ileal sodium/bile acid cotransporter isoform X3
sodium/bile acid cotransporter isoform 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 3 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: 6 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
peptidyl-prolyl cis-trans isomerase-like 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
general transcription factor IIH subunit 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
protein polybromo-1, transcript variant X1
protein polybromo-1, transcript variant X5
protein polybromo-1, transcript variant X2
protein polybromo-1, transcript variant X3
protein polybromo-1, transcript variant X4
protein polybromo-1, transcript variant X7
protein polybromo-1, transcript variant X6
soluble guanylate cyclase 88E, transcript variant X1
soluble guanylate cyclase 88E, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
soluble guanylate cyclase 88E isoform X1
soluble guanylate cyclase 88E isoform X2
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon AGC); 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
28S ribosomal protein S10, mitochondrial
dynein light chain roadblock-type 2-like
dosage compensation regulator, 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 18 samples with support for all annotated introns
dosage compensation regulator, transcript variant X2
dosage compensation regulator isoform X1
dosage compensation regulator isoform X2
protein Skeletor, isoforms B/C, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein Skeletor, isoforms B/C, transcript variant X2
protein Skeletor, isoforms B/C, transcript variant X1
protein Skeletor, isoforms B/C, transcript variant X4
protein Skeletor, isoforms D/E isoform X1
protein Skeletor, isoforms B/C isoform X3
protein Skeletor, isoforms B/C isoform X2
protein Skeletor, isoforms B/C isoform X4
ankyrin repeat domain-containing protein 50, transcript variant X2
ankyrin repeat domain-containing protein 50, transcript variant X1
ankyrin repeat domain-containing protein 50 isoform X2
ankyrin repeat domain-containing protein 50 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 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 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC110991862, transcript variant X1
uncharacterized LOC110991862, transcript variant X2
uncharacterized protein LOC110991862 isoform X1
uncharacterized protein LOC110991862 isoform X2
clathrin interactor 1, transcript variant X1
clathrin interactor 1, transcript variant X2
telomere length regulation protein TEL2 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein Skeletor, isoforms B/C isoform X1
uncharacterized LOC110991637, transcript variant X2
uncharacterized LOC110991637, transcript variant X1
uncharacterized protein LOC110991637 isoform X2
uncharacterized protein LOC110991637 isoform X1
glutamyl-tRNA(Gln) amidotransferase subunit A, mitochondrial
biorientation of chromosomes in cell division protein 1-like 1
succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial-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
28S ribosomal protein S18c, mitochondrial
ABC transporter G family member 23, transcript variant X1
ABC transporter G family member 23 isoform X1
ABC transporter G family member 23, transcript variant X2
ABC transporter G family member 23 isoform X2
protein starmaker, transcript variant X1
protein starmaker, transcript variant X2
cilia- and flagella-associated protein 206
upstream activation factor subunit spp27, transcript variant X2
upstream activation factor subunit spp27, transcript variant X1
upstream activation factor subunit spp27 isoform X2
upstream activation factor subunit spp27 isoform X1
translocator protein, transcript variant X3
translocator protein, transcript variant X5
translocator protein, transcript variant X4
translocator protein, transcript variant X2
translocator protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA isoleucine (anticodon UAU); 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: 2 Proteins, and 5% 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
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
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1
transcription factor BTF3 homolog 4-like
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
beta-1,4-galactosyltransferase 7, transcript variant X2
beta-1,4-galactosyltransferase 7, transcript variant X1
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3, transcript variant X2
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3, transcript variant X3
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3, transcript variant X4
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 isoform X2
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 isoform X4
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 isoform X3
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3, 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 8 samples with support for all annotated introns
nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 isoform X1
zinc finger protein on ecdysone puffs, transcript variant X2
zinc finger protein on ecdysone puffs, transcript variant X1
zinc finger protein on ecdysone puffs, transcript variant X3
zinc finger protein on ecdysone puffs isoform X3
zinc finger protein on ecdysone puffs isoform X2
zinc finger protein on ecdysone puffs isoform X1
large neutral amino acids transporter small subunit 1
NADPH-dependent diflavin oxidoreductase 1, transcript variant X2
NADPH-dependent diflavin oxidoreductase 1, transcript variant X1
NADPH-dependent diflavin oxidoreductase 1 isoform X1
NADPH-dependent diflavin oxidoreductase 1 isoform X2
U3 small nucleolar ribonucleoprotein protein IMP4
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 60 samples with support for all annotated introns
G protein-coupled receptor kinase 2, transcript variant X1
G protein-coupled receptor kinase 2, transcript variant X2
G protein-coupled receptor kinase 2 isoform X1
G protein-coupled receptor kinase 2 isoform X2
methionine--tRNA ligase, mitochondrial, transcript variant X2
methionine--tRNA ligase, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
erythroid differentiation-related factor 1
facilitated trehalose transporter Tret1, transcript variant X1
facilitated trehalose transporter Tret1, 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 101 samples with support for all annotated introns
DNA-directed RNA polymerase I subunit RPA2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
mushroom body large-type Kenyon cell-specific protein 1, transcript variant X1
mushroom body large-type Kenyon cell-specific protein 1, transcript variant X2
mushroom body large-type Kenyon cell-specific protein 1 isoform X1
mushroom body large-type Kenyon cell-specific protein 1 isoform X2
mushroom body large-type Kenyon cell-specific protein 1, transcript variant X3
mushroom body large-type Kenyon cell-specific protein 1 isoform X3
attractin-like protein 1, transcript variant X1
attractin-like protein 1, transcript variant X2
uncharacterized protein LOC111002884 isoform X2
vacuolar protein sorting-associated protein 16B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
vacuolar protein sorting-associated protein 16B, transcript variant X1
vacuolar protein sorting-associated protein 16B
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
facilitated trehalose transporter Tret1 isoform X1
facilitated trehalose transporter Tret1 isoform X2
facilitated trehalose transporter Tret1, transcript variant X3
ornithine transcarbamylase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
probable 28S ribosomal protein S25, mitochondrial
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 10 samples with support for all annotated introns
facilitated trehalose transporter Tret1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ABC transporter G family member 20, transcript variant X1
ABC transporter G family member 20, transcript variant X2
protein phosphatase PP2A 55 kDa regulatory subunit, transcript variant X2
protein phosphatase PP2A 55 kDa regulatory subunit, transcript variant X1
protein phosphatase PP2A 55 kDa regulatory subunit, transcript variant X5
protein phosphatase PP2A 55 kDa regulatory subunit, transcript variant X3
protein phosphatase PP2A 55 kDa regulatory subunit, transcript variant X4
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B alpha isoform isoform X1
protein phosphatase PP2A 55 kDa regulatory subunit isoform X4
protein phosphatase PP2A 55 kDa regulatory subunit isoform X2
protein phosphatase PP2A 55 kDa regulatory subunit isoform X3
cytochrome b-c1 complex subunit 6, mitochondrial
uncharacterized LOC111002872, transcript variant X1
uncharacterized LOC111002872, transcript variant X5
uncharacterized LOC111002872, transcript variant X2
uncharacterized LOC111002872, transcript variant X4
uncharacterized LOC111002872, transcript variant X3
probable small nuclear ribonucleoprotein Sm D2
disintegrin and metalloproteinase domain-containing protein 12
uncharacterized LOC111002901, transcript variant X1
uncharacterized LOC111002901, transcript variant X2
glycerol-3-phosphate acyltransferase 1, mitochondrial, transcript variant X3
glycerol-3-phosphate acyltransferase 1, mitochondrial, transcript variant X2
glycerol-3-phosphate acyltransferase 1, mitochondrial, transcript variant X1
glycerol-3-phosphate acyltransferase 1, mitochondrial isoform X1
glycerol-3-phosphate acyltransferase 1, mitochondrial isoform X2
xenotropic and polytropic retrovirus receptor 1
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
uncharacterized LOC110991864, transcript variant X1
uncharacterized LOC110991864, 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 4 samples with support for all annotated introns
uncharacterized protein LOC110991864 isoform X1
uncharacterized protein LOC110991864 isoform X2
zinc finger protein 771, transcript variant X2
zinc finger protein 771, 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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
equilibrative nucleoside transporter 3, transcript variant X1
equilibrative nucleoside transporter 3, transcript variant X2
uncharacterized LOC110991876, transcript variant X2
uncharacterized LOC110991876, transcript variant X1
uncharacterized protein LOC110991876 isoform X2
uncharacterized protein LOC110991876 isoform X1
vesicular integral-membrane protein VIP36
uncharacterized LOC110991888, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC110991888, transcript variant X2
uncharacterized LOC110991888, 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 30 samples with support for all annotated introns
uncharacterized protein LOC110991888 isoform X1
uncharacterized LOC110991888, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein LOC110991888 isoform X2
FMRFamide receptor-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 12 samples with support for all annotated introns
FMRFamide receptor-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 2 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1, transcript variant X1
serine/arginine repetitive matrix protein 1, transcript variant X2
serine/arginine repetitive matrix protein 1 isoform X1
serine/arginine repetitive matrix protein 1 isoform X2
delta-1-pyrroline-5-carboxylate dehydrogenase, mitochondrial
cell division cycle 7-related protein kinase
CDGSH iron-sulfur domain-containing protein 3, mitochondrial
uncharacterized LOC110991805, transcript variant X9
uncharacterized LOC110991805, transcript variant X5
uncharacterized LOC110991805, transcript variant X3
uncharacterized LOC110991805, transcript variant X4
uncharacterized LOC110991805, transcript variant X1
uncharacterized LOC110991805, transcript variant X8
uncharacterized LOC110991805, transcript variant X2
uncharacterized LOC110991805, transcript variant X6
uncharacterized LOC110991805, transcript variant X7
uncharacterized protein LOC110991805 isoform X1
uncharacterized protein LOC110991805 isoform X3
uncharacterized protein LOC110991805 isoform X4
uncharacterized protein LOC110991805 isoform X8
uncharacterized protein LOC110991805 isoform X2
uncharacterized protein LOC110991805 isoform X6
uncharacterized protein LOC110991805 isoform X7
uncharacterized protein LOC110991805 isoform X5
uncharacterized protein LOC110991805 isoform X9
atrial natriuretic peptide-converting enzyme-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
U11/U12 small nuclear ribonucleoprotein 35 kDa protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
raf homolog serine/threonine-protein kinase Raf
putative uncharacterized protein DDB_G0274435
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
nose resistant to fluoxetine protein 6-like
dual specificity protein phosphatase MPK-4
ecdysone-induced protein 74EF, transcript variant X1
ecdysone-induced protein 74EF, transcript variant X3
ecdysone-induced protein 74EF, transcript variant X2
ecdysone-induced protein 74EF, transcript variant X4
U7 snRNA-associated Sm-like protein LSm11
ecdysone-induced protein 74EF isoform X1
ecdysone-induced protein 74EF isoform X3
ecdysone-induced protein 74EF isoform X2
ecdysone-induced protein 74EF isoform X4
ecdysone-induced protein 74EF, transcript variant X5
ecdysone-induced protein 74EF isoform X5
mitochondrial mRNA pseudouridine synthase Trub2, transcript variant X1
mitochondrial mRNA pseudouridine synthase Trub2, transcript variant X2
mitochondrial mRNA pseudouridine synthase Trub2 isoform X1
mitochondrial mRNA pseudouridine synthase TRUB2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 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 23 samples with support for all annotated introns
uncharacterized protein LOC110991810 isoform X1
uncharacterized protein LOC110991810 isoform X2
uncharacterized protein LOC110991810 isoform X3
ubiquitin carboxyl-terminal hydrolase MINDY-3 homolog, transcript variant X2
ubiquitin carboxyl-terminal hydrolase MINDY-3 homolog, transcript variant X1
ubiquitin carboxyl-terminal hydrolase MINDY-3 homolog
uncharacterized LOC110991859, 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 15 samples with support for all annotated introns
uncharacterized LOC110991859, transcript variant X2
uncharacterized protein LOC110991859 isoform X1
uncharacterized protein LOC110991859 isoform X2
U3 small nucleolar ribonucleoprotein protein IMP3
cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: homeobox protein Nkx-3.1
innexin shaking-B, transcript variant X1
innexin shaking-B, transcript variant X2
innexin shaking-B, transcript variant X3
innexin shaking-B, transcript variant X8
innexin shaking-B, transcript variant X4
innexin shaking-B, transcript variant X10
innexin shaking-B, transcript variant X9
innexin shaking-B, transcript variant X6
innexin shaking-B, transcript variant X5
innexin shaking-B, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
tRNA N(3)-methylcytidine methyltransferase METTL6, transcript variant X3
tRNA N(3)-methylcytidine methyltransferase METTL6, 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 24 samples with support for all annotated introns
tRNA N(3)-methylcytidine methyltransferase METTL6, 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 20 samples with support for all annotated introns
small nucleolar RNA snR60/Z15/Z230/Z193/J17
COORDINATES: nucleotide motif:Rfam:12.0:RF00309
tRNA N(3)-methylcytidine methyltransferase METTL6 isoform X3
tRNA N(3)-methylcytidine methyltransferase METTL6 isoform X2
tRNA N(3)-methylcytidine methyltransferase METTL6 isoform X1
116 kDa U5 small nuclear ribonucleoprotein component
probable low affinity copper uptake protein 2, transcript variant X2
probable low affinity copper uptake protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 92 samples with support for all annotated introns
uncharacterized protein LOC110991886 isoform X1
probable low affinity copper uptake protein 2, transcript variant X3
probable low affinity copper uptake protein 2 isoform X2
folylpolyglutamate synthase, mitochondrial-like, transcript variant X1
folylpolyglutamate synthase, mitochondrial-like, transcript variant X2
folylpolyglutamate synthase, mitochondrial-like isoform X2
folylpolyglutamate synthase, mitochondrial-like isoform X1
folylpolyglutamate synthase, mitochondrial-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 15 samples with support for all annotated introns
folylpolyglutamate synthase, mitochondrial-like isoform X3
putative RNA polymerase II subunit B1 CTD phosphatase RPAP2
histone-lysine N-methyltransferase EHMT1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
histone-lysine N-methyltransferase EHMT1, 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 21 samples with support for all annotated introns
histone-lysine N-methyltransferase EHMT1 isoform X1
histone-lysine N-methyltransferase EHMT1 isoform X2
spectrin alpha chain, transcript variant X4
spectrin alpha chain, transcript variant X3
spectrin alpha chain, transcript variant X2
spectrin alpha chain, transcript variant X1
homeobox protein extradenticle, transcript variant X2
homeobox protein extradenticle, transcript variant X1
homeobox protein extradenticle, transcript variant X4
homeobox protein extradenticle, transcript variant X3
homeobox protein extradenticle isoform X4
homeobox protein extradenticle isoform X3
homeobox protein extradenticle isoform X2
homeobox protein extradenticle isoform X1
pre-mRNA-splicing factor 38B, transcript variant X1
pre-mRNA-splicing factor 38B, 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 33 samples with support for all annotated introns
ubiquitin-like protein 5, transcript variant X2
ubiquitin-like protein 5, transcript variant X1
ubiquitin-like protein 5, transcript variant X4
ubiquitin-like protein 5, transcript variant X5
ubiquitin-like protein 5, transcript variant X3
iron-sulfur protein NUBPL, transcript variant X2
iron-sulfur protein NUBPL, transcript variant X1
uncharacterized LOC110991837, transcript variant X1
uncharacterized LOC110991837, transcript variant X3
uncharacterized LOC110991837, transcript variant X2
uncharacterized protein LOC110991837 isoform X1
uncharacterized protein LOC110991837 isoform X2
BTB/POZ and MATH domain-containing 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 109 samples with support for all annotated introns
uncharacterized LOC110991868, transcript variant X2
uncharacterized LOC110991868, 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 85 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB9
40S ribosomal protein S23, transcript variant X2
40S ribosomal protein S23, transcript variant X1
receptor-mediated endocytosis protein 6 homolog, transcript variant X2
receptor-mediated endocytosis protein 6 homolog, transcript variant X1
receptor-mediated endocytosis protein 6 homolog isoform X2
receptor-mediated endocytosis protein 6 homolog isoform X1
dual specificity mitogen-activated protein kinase kinase 7, transcript variant X1
dual specificity mitogen-activated protein kinase kinase 7, transcript variant X2
dual specificity mitogen-activated protein kinase kinase 7 isoform X1
dual specificity mitogen-activated protein kinase kinase 7 isoform X2
uridine-cytidine kinase, transcript variant X1
uridine-cytidine kinase, transcript variant X2
amidophosphoribosyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
amidophosphoribosyltransferase, 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 18 samples with support for all annotated introns
amidophosphoribosyltransferase, transcript variant X2
amidophosphoribosyltransferase isoform X1
amidophosphoribosyltransferase isoform X2
casein kinase II subunit beta-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
casein kinase II subunit beta-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 78 samples with support for all annotated introns
casein kinase II subunit beta-like isoform X1
casein kinase II subunit beta-like isoform X2
casein kinase II subunit beta, transcript variant X1
casein kinase II subunit beta, transcript variant X2
uncharacterized LOC111000670, transcript variant X2
uncharacterized LOC111000670, transcript variant X4
uncharacterized LOC111000670, transcript variant X1
uncharacterized LOC111000670, transcript variant X5
uncharacterized LOC111000670, transcript variant X3
cysteine-rich with EGF-like domain protein 2, transcript variant X1
cysteine-rich with EGF-like domain protein 2, 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 27 samples with support for all annotated introns
cysteine-rich with EGF-like domain protein 2 isoform X1
cysteine-rich with EGF-like domain protein 2 isoform X2
uncharacterized protein LOC111000670 isoform X1
uncharacterized protein LOC111000670 isoform X2
uncharacterized LOC111000695, 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
uncharacterized LOC111000695, transcript variant X1
uncharacterized LOC111000695, transcript variant X4
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
uncharacterized protein LOC111000695 isoform X2
uncharacterized protein LOC111000695 isoform X1
uncharacterized protein LOC111000695 isoform X4
uncharacterized LOC111000695, transcript variant X3
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
uncharacterized protein LOC111000695 isoform X3
uncharacterized LOC111000695, transcript variant X5
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 2 samples with support for all annotated introns
uncharacterized protein LOC111000695 isoform X5
prion-like-(Q/N-rich) domain-bearing protein 25, transcript variant X2
prion-like-(Q/N-rich) domain-bearing protein 25, transcript variant X3
prion-like-(Q/N-rich) domain-bearing protein 25, transcript variant X1
prion-like-(Q/N-rich) domain-bearing protein 25
neurogenic locus Notch protein, transcript variant X2
neurogenic locus Notch protein, transcript variant X1
neurogenic locus Notch protein isoform X2
neurogenic locus Notch protein isoform X1
putative golgin subfamily A member 6-like protein 3
neuropathy target esterase sws, transcript variant X2
neuropathy target esterase sws, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
neuropathy target esterase sws, transcript variant X4
neuropathy target esterase sws, 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 16 samples with support for all annotated introns
neuropathy target esterase sws, transcript variant X3
neuropathy target esterase sws, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
neuropathy target esterase sws, transcript variant X6
neuropathy target esterase sws isoform X5
neuropathy target esterase sws isoform X2
neuropathy target esterase sws isoform X4
neuropathy target esterase sws isoform X1
neuropathy target esterase sws isoform X3
neuropathy target esterase sws isoform X6
RNA-binding protein 1, transcript variant X1
RNA-binding protein 1, transcript variant X2
RNA-binding protein 1, transcript variant X3
RNA-binding protein 1, 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 97 samples with support for all annotated introns
UDP-xylose and UDP-N-acetylglucosamine transporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
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 20 samples with support for all annotated introns
uncharacterized LOC111000694, transcript variant X2
uncharacterized protein LOC111000694 isoform X2
uncharacterized LOC111000694, transcript variant X1
uncharacterized protein LOC111000694 isoform X1
uncharacterized LOC123690378, transcript variant X1
uncharacterized LOC123690378, transcript variant X2
uncharacterized protein LOC123690378 isoform X1
uncharacterized protein LOC123690378 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00049
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase SMYD3, 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 8 samples with support for all annotated introns
histone-lysine N-methyltransferase SMYD3, transcript variant X4
histone-lysine N-methyltransferase SMYD3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
histone-lysine N-methyltransferase SMYD3, transcript variant X1
histone-lysine N-methyltransferase SMYD3 isoform X1
histone-lysine N-methyltransferase SMYD3 isoform X2
uncharacterized protein C1orf131 homolog
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 76 samples with support for all annotated introns
uncharacterized LOC111000669, 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 34 samples with support for all annotated introns
uncharacterized LOC111000669, transcript variant X2
uncharacterized protein LOC111000669 isoform X1
uncharacterized protein LOC111000669 isoform X2
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
UPF0605 protein CG18335-like, transcript variant X1
UPF0605 protein CG18335-like, transcript variant X2
kynurenine aminotransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 86 samples with support for all annotated introns
kynurenine aminotransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 110 samples with support for all annotated introns
kynurenine aminotransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 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: 30 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: 17 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chymotrypsin-2-like, transcript variant X1
chymotrypsin-2-like, transcript variant X2
chymotrypsin-1-like, transcript variant X1
chymotrypsin-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
chymotrypsin-1-like, transcript variant X3
chymotrypsin-1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 4 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: kallikrein 1-related peptidase b9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 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 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC111002781, transcript variant X2
uncharacterized LOC111002781, transcript variant X1
uncharacterized LOC111002781, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: chymotrypsin-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
deoxynucleotidyltransferase terminal-interacting protein 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 55 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 109 samples with support for all annotated introns
nuclear hormone receptor FTZ-F1 beta, 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 28 samples with support for all annotated introns
nuclear hormone receptor FTZ-F1 beta, transcript variant X1
nuclear hormone receptor FTZ-F1 beta isoform X2
nuclear hormone receptor FTZ-F1 beta isoform X1
ras-related protein Rab-9B, transcript variant X1
ras-related protein Rab-9B, transcript variant X2
serine/arginine repetitive matrix protein 2, transcript variant X3
serine/arginine repetitive matrix protein 2, transcript variant X4
serine/arginine repetitive matrix protein 2, transcript variant X1
serine/arginine repetitive matrix protein 2, transcript variant X2
serine/arginine repetitive matrix protein 2 isoform X3
uncharacterized protein LOC110999170 isoform X4
serine/arginine repetitive matrix protein 2 isoform X1
serine/arginine repetitive matrix protein 2 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 7 samples with support for all annotated introns
rab GTPase-activating protein 1-like, transcript variant X2
rab GTPase-activating protein 1-like, transcript variant X1
rab GTPase-activating protein 1-like, transcript variant X4
rab GTPase-activating protein 1-like, transcript variant X5
rab GTPase-activating protein 1-like isoform X2
rab GTPase-activating protein 1-like isoform X1
rab GTPase-activating protein 1-like isoform X4
rab GTPase-activating protein 1-like isoform X5
rab GTPase-activating protein 1-like, 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 21 samples with support for all annotated introns
rab GTPase-activating protein 1-like isoform 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 26 samples with support for all annotated introns
stress-activated map kinase-interacting protein 1
dynein light chain Tctex-type protein 2B, transcript variant X2
dynein light chain Tctex-type protein 2B, 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 38 samples with support for all annotated introns
SET and MYND domain-containing protein 4
dynein light chain Tctex-type protein 2B
aquaporin AQPAe.a, transcript variant X2
aquaporin AQPAe.a, transcript variant X1
aquaporin AQPAe.a, transcript variant X3
aquaporin AQPAe.a, transcript variant X4
E3 ubiquitin-protein ligase UBR4, transcript variant X3
E3 ubiquitin-protein ligase UBR4, transcript variant X2
E3 ubiquitin-protein ligase UBR4, transcript variant X1
E3 ubiquitin-protein ligase UBR4 isoform X3
E3 ubiquitin-protein ligase UBR4 isoform X2
E3 ubiquitin-protein ligase UBR4 isoform X1