Drosophila subpulchrella strain 33 F10 #4 breed RU33 chromosome 4, RU_Dsub_v1.1 Primary Assembly, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Holometabola; Diptera; Brachycera; Muscomorpha; Ephydroidea; Drosophilidae; Drosophila; Sophophora.
REFSEQ INFORMATION: The reference sequence is identical to\nCM025932.1.\nAssembly name: RU_Dsub_v1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by The Rockefeller University on\n2020/10/02. The original whole-genome shotgun project has the\naccession JACOEE000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: The Rockefeller University\nAssembly Method :: Canu v. 1.7\nAssembly Name :: RU_Dsub_v1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 260.0x\nSequencing Technology :: Illumina HiSeq; PacBio Sequel\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Drosophila subpulchrella Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.5\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.
calcium-dependent secretion activator, transcript variant X8
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
calcium-dependent secretion activator, 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 10 samples with support for all annotated introns
calcium-dependent secretion activator, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
calcium-dependent secretion activator, transcript variant X6
calcium-dependent secretion activator, transcript variant X5
calcium-dependent secretion activator, transcript variant X3
calcium-dependent secretion activator, transcript variant X2
calcium-dependent secretion activator, transcript variant X7
calcium-dependent secretion activator, transcript variant X10
calcium-dependent secretion activator, transcript variant X9
calcium-dependent secretion activator, transcript variant X1
calcium-dependent secretion activator isoform X2
calcium-dependent secretion activator isoform X5
calcium-dependent secretion activator isoform X4
calcium-dependent secretion activator isoform X3
calcium-dependent secretion activator isoform X1
calcium-dependent secretion activator isoform X6
metabotropic glutamate receptor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
metabotropic glutamate receptor, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
metabotropic glutamate receptor, transcript variant X3
metabotropic glutamate receptor, 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 3 samples with support for all annotated introns
metabotropic glutamate receptor, transcript variant X2
metabotropic glutamate receptor isoform X1
metabotropic glutamate receptor isoform X2
metabotropic glutamate receptor 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 10 samples with support for all annotated introns
uncharacterized LOC119563427, transcript variant X5
uncharacterized LOC119563427, 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 2 samples with support for all annotated introns
uncharacterized LOC119563427, transcript variant X3
uncharacterized LOC119563427, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119563427, transcript variant X2
uncharacterized protein LOC119563427 isoform X2
uncharacterized protein LOC119563427 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC119545857, 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 3 samples with support for all annotated introns
uncharacterized LOC119545857, transcript variant X4
uncharacterized LOC119545857, transcript variant X1
uncharacterized LOC119545857, transcript variant X2
uncharacterized protein LOC119545857 isoform X2
uncharacterized protein LOC119545857 isoform X3
uncharacterized protein LOC119545857 isoform X1
paired box protein Pax-6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
paired box protein Pax-6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 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: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ATP synthase subunit beta, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X8
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 10 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X1
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X2
calcium/calmodulin-dependent protein kinase type II alpha chain isoform X8
calcium/calmodulin-dependent protein kinase type II alpha chain isoform X7
calcium/calmodulin-dependent protein kinase type II alpha chain isoform X6
calcium/calmodulin-dependent protein kinase type II alpha chain isoform X4
calcium/calmodulin-dependent protein kinase type II alpha chain isoform X3
calcium/calmodulin-dependent protein kinase type II alpha chain isoform X5
calcium/calmodulin-dependent protein kinase type II alpha chain isoform X2
calcium/calmodulin-dependent protein kinase type II alpha chain isoform X1
calcium/calmodulin-dependent protein kinase type II alpha 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 8 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II alpha chain, transcript variant X12
calcium/calmodulin-dependent protein kinase type II alpha chain isoform X11
calcium/calmodulin-dependent protein kinase type II alpha chain isoform X10
calcium/calmodulin-dependent protein kinase type II alpha chain isoform X9
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 9 samples with support for all annotated introns
LIM domain-containing protein C4F6.12 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC119562898 isoform X5
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 10 samples with support for all annotated introns
inhibin beta chain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
inhibin beta chain, 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 10 samples with support for all annotated introns
inhibin beta chain, 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 6 samples with support for all annotated introns
paired box protein Pax-5, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
paired box protein Pax-5, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
paired box protein Pax-5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
paired box protein Pax-5, transcript variant X1
putative uncharacterized protein DDB_G0282133 isoform X2
paired box protein Pax-5, transcript variant X2
putative uncharacterized protein DDB_G0277255 isoform X1
paired box protein Pax-5, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
paired box protein Pax-5, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2 isoform X1
glutamate receptor ionotropic, kainate 1 isoform X4
glutamate receptor ionotropic, kainate 2 isoform X3
glutamate receptor ionotropic, kainate 2 isoform X6
glutamate receptor ionotropic, kainate 2 isoform X2
glutamate receptor ionotropic, kainate 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 2 isoform X5
uncharacterized LOC119551223, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC119551223, transcript variant X4
uncharacterized LOC119551223, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC119551223, 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 9 samples with support for all annotated introns
uncharacterized LOC119551223, transcript variant X3
uncharacterized LOC119551223, transcript variant X2
osmotic avoidance abnormal protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
osmotic avoidance abnormal protein 3, transcript variant X2
osmotic avoidance abnormal protein 3, transcript variant X6
osmotic avoidance abnormal protein 3, transcript variant X3
osmotic avoidance abnormal protein 3, transcript variant X10
osmotic avoidance abnormal protein 3, transcript variant X5
osmotic avoidance abnormal protein 3, transcript variant X9
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
osmotic avoidance abnormal protein 3, transcript variant X7
osmotic avoidance abnormal protein 3, transcript variant X11
osmotic avoidance abnormal protein 3, 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 1 sample with support for all annotated introns
osmotic avoidance abnormal protein 3 isoform X2
osmotic avoidance abnormal protein 3 isoform X1
osmotic avoidance abnormal protein 3 isoform X4
osmotic avoidance abnormal protein 3 isoform X3
osmotic avoidance abnormal protein 3 isoform X6
osmotic avoidance abnormal protein 3 isoform X5
osmotic avoidance abnormal protein 3 isoform X7
osmotic avoidance abnormal protein 3, transcript variant X8
osmotic avoidance abnormal protein 3 isoform X8
polycomb protein PHO, transcript variant X1
polycomb protein PHO, transcript variant X2
LIM domain and actin-binding protein 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LIM domain and actin-binding protein 1, transcript variant X5
LIM domain and actin-binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LIM domain and actin-binding protein 1, transcript variant X2
LIM domain and actin-binding protein 1, 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 4 samples with support for all annotated introns
LIM domain and actin-binding protein 1 isoform X2
uncharacterized protein LOC119556706 isoform X1
uncharacterized protein LOC119556706 isoform X4
LIM domain and actin-binding protein 1, transcript variant X3
LIM domain and actin-binding protein 1 isoform X3
LIM domain and actin-binding protein 1 isoform X5
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X2
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X1
phosphatidylinositol 5-phosphate 4-kinase type-2 beta, transcript variant X3
phosphatidylinositol 5-phosphate 4-kinase type-2 beta
microphthalmia-associated transcription factor, transcript variant X8
microphthalmia-associated transcription factor, transcript variant X4
microphthalmia-associated transcription factor isoform X3
microphthalmia-associated transcription factor isoform X6
microphthalmia-associated transcription factor, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
microphthalmia-associated transcription factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
microphthalmia-associated transcription factor, transcript variant X2
microphthalmia-associated transcription factor, transcript variant X3
microphthalmia-associated transcription factor isoform X1
microphthalmia-associated transcription factor isoform X2
microphthalmia-associated transcription factor, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
microphthalmia-associated transcription factor, transcript variant X6
microphthalmia-associated transcription factor isoform X4
putative dual specificity tyrosine-phosphorylation-regulated kinase 3 homolog, transcript variant X2
putative dual specificity tyrosine-phosphorylation-regulated kinase 3 homolog, transcript variant X1
putative dual specificity tyrosine-phosphorylation-regulated kinase 3 homolog
eukaryotic translation initiation factor 4 gamma 3, transcript variant X1
eukaryotic translation initiation factor 4 gamma 3, transcript variant X2
eukaryotic translation initiation factor 4 gamma 3 isoform X1
eukaryotic translation initiation factor 4 gamma 3 isoform X2
eukaryotic translation initiation factor 4 gamma 3, transcript variant X3
eukaryotic translation initiation factor 4 gamma 3 isoform X3
uncharacterized LOC119546202, transcript variant X8
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
uncharacterized LOC119546202, transcript variant X10
uncharacterized LOC119546202, transcript variant X14
uncharacterized LOC119546202, transcript variant X11
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 9 samples with support for all annotated introns
uncharacterized LOC119546202, transcript variant X13
uncharacterized LOC119546202, transcript variant X12
uncharacterized LOC119546202, transcript variant X9
uncharacterized protein LOC119546202 isoform X8
uncharacterized protein LOC119546202 isoform X10
uncharacterized protein LOC119546202 isoform X12
uncharacterized protein LOC119546202 isoform X11
uncharacterized protein LOC119546202 isoform X9
uncharacterized protein LOC119546202 isoform X13
uncharacterized LOC119546202, transcript variant X16
uncharacterized LOC119546202, transcript variant X17
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
uncharacterized LOC119546202, transcript variant X15
uncharacterized LOC119546202, 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 9 samples with support for all annotated introns
uncharacterized LOC119546202, 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 8 samples with support for all annotated introns
uncharacterized LOC119546202, transcript variant X1
uncharacterized LOC119546202, 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 5 samples with support for all annotated introns
uncharacterized LOC119546202, transcript variant X6
uncharacterized LOC119546202, transcript variant X5
uncharacterized LOC119546202, transcript variant X4
uncharacterized protein LOC119546202 isoform X2
uncharacterized protein LOC119546202 isoform X1
uncharacterized protein LOC119546202 isoform X5
uncharacterized protein LOC119546202 isoform X4
uncharacterized protein LOC119546202 isoform X3
uncharacterized protein LOC119546202 isoform X7
uncharacterized protein LOC119546202 isoform X6
uncharacterized protein LOC119546202 isoform X14
uncharacterized protein LOC119546202 isoform X15
GIGYF family protein CG11148, transcript variant X2
GIGYF family protein CG11148, 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 4 samples with support for all annotated introns
transcription factor SOX-6, transcript variant X1
transcription factor SOX-6, 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
transcription factor SOX-6, transcript variant X4
transcription factor SOX-6, transcript variant X3
transcription factor SOX-6, transcript variant X5
mediator of RNA polymerase II transcription subunit 26, transcript variant X1
mediator of RNA polymerase II transcription subunit 26, transcript variant X3
mediator of RNA polymerase II transcription subunit 26, 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 9 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 26 isoform X1
mediator of RNA polymerase II transcription subunit 26 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 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: 18 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: 19 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: 18 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: 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: 18 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: 18 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
growth/differentiation factor 8, transcript variant X2
growth/differentiation factor 8, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
growth/differentiation factor 8, transcript variant X1
growth/differentiation factor 8, transcript variant X4
growth/differentiation factor 8, transcript variant X5
growth/differentiation factor 8 isoform X2
growth/differentiation factor 8 isoform X3
uncharacterized protein LOC119562574 isoform X1
RNA-binding protein MEX3B, transcript variant X5
RNA-binding protein MEX3B, transcript variant X2
RNA-binding protein MEX3B, transcript variant X3
RNA-binding protein MEX3B, transcript variant X1
RNA-binding protein MEX3B, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 1 isoform X1
sodium- and chloride-dependent GABA transporter 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
sodium- and chloride-dependent GABA transporter 1 isoform X2
ephrin type-B receptor 1-B, transcript variant X3
ephrin type-B receptor 1-B, transcript variant X4
ephrin type-B receptor 1-B, transcript variant X2
ephrin type-B receptor 1-B, transcript variant X5
ephrin type-B receptor 1-B, transcript variant X1
ephrin type-B receptor 1-B, transcript variant X6
43 kDa receptor-associated protein of the synapse, transcript variant X1
43 kDa receptor-associated protein of the synapse, transcript variant X2
43 kDa receptor-associated protein of the synapse isoform X1
43 kDa receptor-associated protein of the synapse homolog isoform X2
uncharacterized LOC119563161, 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 5 samples with support for all annotated introns
uncharacterized protein LOC119563161 isoform X2
uncharacterized LOC119563161, transcript variant X1
uncharacterized LOC119563161, 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 6 samples with support for all annotated introns
uncharacterized protein LOC119563161 isoform X1
NADH-ubiquinone oxidoreductase 49 kDa subunit
transcriptional activator protein Pur-beta, transcript variant X2
transcriptional activator protein Pur-beta, transcript variant X3
transcriptional activator protein Pur-beta, transcript variant X1
transcriptional activator protein Pur-beta isoform X2
transcriptional activator protein Pur-alpha isoform X1
uncharacterized LOC119552166, transcript variant X2
uncharacterized LOC119552166, transcript variant X1
uncharacterized LOC119552166, transcript variant X3
uncharacterized protein LOC119552166 isoform X1
uncharacterized protein LOC119552166 isoform X2
zinc finger protein 2, transcript variant X6
zinc finger protein 2, transcript variant X5
zinc finger protein 2, transcript variant X4
zinc finger protein 2, 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 3 samples with support for all annotated introns
zinc finger protein 2, transcript variant X7
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
zinc finger protein 2, 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 4 samples with support for all annotated introns
zinc finger protein 2, 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 2 samples with support for all annotated introns
zinc finger protein 2, transcript variant X8
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
tau-tubulin kinase homolog Asator, transcript variant X1
tau-tubulin kinase homolog Asator, transcript variant X5
tau-tubulin kinase homolog Asator, transcript variant X3
tau-tubulin kinase homolog Asator, transcript variant X4
tau-tubulin kinase homolog Asator, 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 7 samples with support for all annotated introns
tau-tubulin kinase homolog Asator isoform X1
tau-tubulin kinase homolog Asator isoform X4
tau-tubulin kinase homolog Asator isoform X2
tau-tubulin kinase homolog Asator isoform X3
uncharacterized LOC119561989, transcript variant X2
uncharacterized LOC119561989, transcript variant X1
uncharacterized LOC119561989, transcript variant X3
transcription initiation factor TFIID subunit 3, transcript variant X1
transcription initiation factor TFIID subunit 3, transcript variant X2
transcription initiation factor TFIID subunit 3 isoform X1
transcription initiation factor TFIID subunit 3 isoform X2
calcium/calmodulin-dependent protein kinase type 1, transcript variant X3
calcium/calmodulin-dependent protein kinase type 1, transcript variant X1
calcium/calmodulin-dependent protein kinase type 1, transcript variant X2
calcium/calmodulin-dependent protein kinase type 1 isoform X2
calcium/calmodulin-dependent protein kinase type 1 isoform X1
uncharacterized LOC119553809, transcript variant X1
uncharacterized LOC119553809, transcript variant X3
uncharacterized LOC119553809, transcript variant X2
uncharacterized LOC119553809, transcript variant X4
uncharacterized LOC119553809, transcript variant X5
zinc finger protein 646, transcript variant X4
zinc finger protein 646, transcript variant X5
zinc finger protein 646, transcript variant X6
zinc finger protein 646, transcript variant X1
zinc finger protein 646, transcript variant X3
zinc finger protein 646, transcript variant X2
uncharacterized protein LOC119560367 isoform X1
uncharacterized protein LOC119560367 isoform X3
uncharacterized protein LOC119560367 isoform X4
uncharacterized protein LOC119560367 isoform X2
uncharacterized protein LOC119560367 isoform X5
zinc finger protein 646, transcript variant X14
zinc finger protein 646, transcript variant X12
zinc finger protein 646, transcript variant X13
zinc finger protein 646, transcript variant X7
zinc finger protein 646, transcript variant X8
zinc finger protein 646, transcript variant X11
zinc finger protein 646, transcript variant X10
uncharacterized protein LOC119560367 isoform X6
zinc finger protein 646, transcript variant X9
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
plasma membrane calcium-transporting ATPase 3, transcript variant X4
plasma membrane calcium-transporting ATPase 3, transcript variant X5
plasma membrane calcium-transporting ATPase 3, transcript variant X8
plasma membrane calcium-transporting ATPase 3, transcript variant X6
plasma membrane calcium-transporting ATPase 3, transcript variant X9
plasma membrane calcium-transporting ATPase 3, transcript variant X7
plasma membrane calcium-transporting ATPase 3, transcript variant X10
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
plasma membrane calcium-transporting ATPase 3, transcript variant X11
plasma membrane calcium-transporting ATPase 3, transcript variant X1
plasma membrane calcium-transporting ATPase 3, transcript variant X2
plasma membrane calcium-transporting ATPase 3, transcript variant X3
plasma membrane calcium-transporting ATPase 3, transcript variant X14
plasma membrane calcium-transporting ATPase 3, transcript variant X15
plasma membrane calcium-transporting ATPase 3, transcript variant X13
plasma membrane calcium-transporting ATPase 3, transcript variant X12
plasma membrane calcium-transporting ATPase 2 isoform X4
plasma membrane calcium-transporting ATPase 2 isoform X7
plasma membrane calcium-transporting ATPase 2 isoform X5
plasma membrane calcium-transporting ATPase 2 isoform X8
plasma membrane calcium-transporting ATPase 2 isoform X6
plasma membrane calcium-transporting ATPase 2 isoform X9
plasma membrane calcium-transporting ATPase 2 isoform X10
plasma membrane calcium-transporting ATPase 2 isoform X1
plasma membrane calcium-transporting ATPase 2 isoform X2
plasma membrane calcium-transporting ATPase 2 isoform X3
plasma membrane calcium-transporting ATPase 3 isoform X13
plasma membrane calcium-transporting ATPase 3 isoform X14
plasma membrane calcium-transporting ATPase 3 isoform X12
plasma membrane calcium-transporting ATPase 2 isoform X11
RING finger protein 11, transcript variant X4
RING finger protein 11, transcript variant X3
RING finger protein 11, transcript variant X2
RING finger protein 11, transcript variant X1
RING finger protein 11, transcript variant X5
RING finger protein 11, transcript variant X6
zinc transporter ZIP9-B, transcript variant X2
zinc transporter ZIP9-B, transcript variant X1
UV excision repair protein RAD23 homolog A
nuclear factor 1 C-type, transcript variant X4
nuclear factor 1 C-type, transcript variant X3
nuclear factor 1 C-type, transcript variant X1
nuclear factor 1 C-type, 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 8 samples with support for all annotated introns
nuclear factor 1 C-type, transcript variant X5
rho GTPase-activating protein 6, transcript variant X6
rho GTPase-activating protein 6, transcript variant X1
rho GTPase-activating protein 6, transcript variant X2
uncharacterized protein LOC119551734 isoform X2
uncharacterized protein LOC119551734 isoform X1
rho GTPase-activating protein 6 isoform X5
rho GTPase-activating protein 6, transcript variant X3
rho GTPase-activating protein 6, transcript variant X5
uncharacterized protein LOC119551734 isoform X4
rho GTPase-activating protein 6, transcript variant X4
uncharacterized protein LOC119551734 isoform X3
uncharacterized LOC119552088, transcript variant X2
uncharacterized LOC119552088, transcript variant X1
kinesin-related protein 4, transcript variant X7
kinesin-related protein 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
kinesin-related protein 4, transcript variant X4
kinesin-related protein 4, transcript variant X3
kinesin-related protein 4, transcript variant X1
kinesin-related protein 4, transcript variant X11
kinesin-related protein 4, transcript variant X10
kinesin-related protein 4, transcript variant X6
kinesin-related protein 4, transcript variant X8
kinesin-related protein 4, transcript variant X9
kinesin-related protein 4, transcript variant X2
kinesin-related protein 4, transcript variant X14
kinesin-related protein 4, transcript variant X12
uncharacterized protein LOC119562996 isoform X7
uncharacterized protein LOC119562996 isoform X9
uncharacterized protein LOC119562996 isoform X6
uncharacterized protein LOC119562996 isoform X4
uncharacterized protein LOC119562996 isoform X2
uncharacterized protein LOC119562996 isoform X8
uncharacterized protein LOC119562996 isoform X3
uncharacterized protein LOC119562996 isoform X1
uncharacterized protein LOC119562996 isoform X11
uncharacterized protein LOC119562996 isoform X10
kinesin-related protein 4, transcript variant X15
kinesin-related protein 4, transcript variant X13
kinesin-related protein 4, transcript variant X16
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
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 10 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 4 samples with support for all annotated introns
uncharacterized LOC119563122, transcript variant X8
uncharacterized LOC119563122, transcript variant X5
uncharacterized LOC119563122, transcript variant X6
uncharacterized LOC119563122, transcript variant X7
uncharacterized LOC119563122, transcript variant X3
uncharacterized LOC119563122, transcript variant X2
uncharacterized LOC119563122, transcript variant X1
uncharacterized LOC119563122, transcript variant X4
adapter molecule Crk, transcript variant X1
adapter molecule Crk, transcript variant X2
ATP-binding cassette sub-family D member
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 10 samples with support for all annotated introns
ADP-ribosylation factor-like protein 4A, transcript variant X4
ADP-ribosylation factor-like protein 4A, transcript variant X2
ADP-ribosylation factor-like protein 4A, 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
ADP-ribosylation factor-like protein 4A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ADP-ribosylation factor-like protein 4A isoform X1
ADP-ribosylation factor-like protein 4A isoform X3
ADP-ribosylation factor-like protein 4C isoform X4
ADP-ribosylation factor-like protein 4A isoform X2
uncharacterized LOC119548648, transcript variant X2
uncharacterized LOC119548648, transcript variant X1
uncharacterized LOC119548648, transcript variant X3
uncharacterized LOC119558332, 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
uncharacterized LOC119558332, transcript variant X3
uncharacterized LOC119558332, transcript variant X2
uncharacterized LOC119558332, transcript variant X1
uncharacterized protein LOC119558332 isoform X2
uncharacterized protein LOC119558332 isoform X1
uncharacterized protein LOC119558332 isoform X3
uncharacterized LOC119558188, transcript variant X3
uncharacterized protein LOC119558188 isoform X3
uncharacterized LOC119558188, transcript variant X2
uncharacterized LOC119558188, transcript variant X1
uncharacterized protein LOC119558188 isoform X2
uncharacterized protein LOC119558188 isoform X1
probable cation-transporting ATPase 13A3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable cation-transporting ATPase 13A3
protein pangolin, isoforms A/H/I/S, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
protein pangolin, isoforms A/H/I/S, transcript variant X12
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
protein pangolin, isoforms A/H/I/S, 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 5 samples with support for all annotated introns
protein pangolin, isoforms A/H/I/S, 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 3 samples with support for all annotated introns
protein pangolin, isoforms A/H/I/S, 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 9 samples with support for all annotated introns
protein pangolin, isoforms A/H/I/S, transcript variant X15
protein pangolin, isoforms A/H/I/S, transcript variant X10
protein pangolin, isoforms A/H/I/S, transcript variant X9
protein pangolin, isoforms A/H/I/S, transcript variant X8
protein pangolin, isoforms A/H/I/S, transcript variant X11
protein pangolin, isoforms A/H/I/S, transcript variant X7
protein pangolin, isoforms A/H/I/S isoform X9
protein pangolin, isoforms A/H/I/S isoform X8
protein pangolin, isoforms A/H/I/S isoform X7
protein pangolin, isoforms A/H/I/S isoform X6
protein pangolin, isoforms A/H/I/S isoform X11
protein pangolin, isoforms A/H/I/S, transcript variant X4
protein pangolin, isoforms A/H/I/S, transcript variant X5
protein pangolin, isoforms A/H/I/S, transcript variant X6
protein pangolin, isoforms A/H/I/S, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
protein pangolin, isoforms A/H/I/S isoform X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
transcriptional activator cubitus interruptus, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transcriptional activator cubitus interruptus, transcript variant X2
transcriptional activator cubitus interruptus isoform X2
transcriptional activator cubitus interruptus, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
transcriptional activator cubitus interruptus, transcript variant X1
transcriptional activator cubitus interruptus isoform X1
transcriptional activator cubitus interruptus isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119557675, transcript variant X3
uncharacterized LOC119557675, transcript variant X2
uncharacterized LOC119557675, transcript variant X4
uncharacterized LOC119557675, transcript variant X1
uncharacterized protein LOC119557675 isoform X2
uncharacterized protein LOC119557675 isoform X1
sodium/potassium-transporting ATPase subunit alpha