Portunus trituberculatus isolate SZX2019 chromosome 33, ASM1759143v1, whole genome shotgun sequence.
Portunus trituberculatus (swimming crab)
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Crustacea; Multicrustacea; Malacostraca; Eumalacostraca; Eucarida; Decapoda; Pleocyemata; Brachyura; Eubrachyura; Portunoidea; Portunidae; Portunus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM030103.1.\nAssembly name: ASM1759143v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Center for Ecological and\nEnvironmental Sciences on 2021/03/30. The original whole-genome\nshotgun project has the accession JAGGDN000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Center for Ecological and Environmental\n Sciences\nAssembly Method :: Wtdbg v. 2.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 54.74x\nSequencing Technology :: Oxford Nanopore; Illumina\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Portunus trituberculatus Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: COP1-interactive protein 1-like
COORDINATES: polyA evidence [ECO:0006239]
methionine adenosyltransferase 2 subunit beta-like, transcript variant X2
methionine adenosyltransferase 2 subunit beta-like, transcript variant X3
methionine adenosyltransferase 2 subunit beta-like, transcript variant X1
methionine adenosyltransferase 2 subunit beta-like isoform X2
methionine adenosyltransferase 2 subunit beta-like isoform X1
complex III assembly factor LYRM7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
complex III assembly factor LYRM7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
complex III assembly factor LYRM7-like isoform X1
complex III assembly factor LYRM7-like isoform X2
ankyrin repeat domain-containing protein 13C-like, transcript variant X2
ankyrin repeat domain-containing protein 13C-like, transcript variant X1
ankyrin repeat domain-containing protein 13C-like isoform X2
ankyrin repeat domain-containing protein 13C-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
CUGBP Elav-like family member 4, transcript variant X3
CUGBP Elav-like family member 4, transcript variant X10
CUGBP Elav-like family member 4, transcript variant X16
CUGBP Elav-like family member 4, transcript variant X7
CUGBP Elav-like family member 4, transcript variant X21
CUGBP Elav-like family member 4, transcript variant X9
CUGBP Elav-like family member 4, transcript variant X27
CUGBP Elav-like family member 4, transcript variant X12
CUGBP Elav-like family member 4, transcript variant X32
CUGBP Elav-like family member 4, transcript variant X30
CUGBP Elav-like family member 4, transcript variant X15
CUGBP Elav-like family member 4 isoform X3
CUGBP Elav-like family member 4 isoform X7
CUGBP Elav-like family member 4 isoform X19
CUGBP Elav-like family member 4 isoform X9
CUGBP Elav-like family member 4 isoform X11
CUGBP Elav-like family member 4 isoform X29
CUGBP Elav-like family member 4 isoform X14
CUGBP Elav-like family member 4 isoform X24
CUGBP Elav-like family member 4 isoform X27
CUGBP Elav-like family member 4, transcript variant X11
CUGBP Elav-like family member 4, transcript variant X14
CUGBP Elav-like family member 4, transcript variant X17
CUGBP Elav-like family member 4, transcript variant X31
CUGBP Elav-like family member 4, transcript variant X34
CUGBP Elav-like family member 4, transcript variant X22
CUGBP Elav-like family member 4, transcript variant X2
CUGBP Elav-like family member 4, transcript variant X13
CUGBP Elav-like family member 4, transcript variant X33
CUGBP Elav-like family member 4, transcript variant X35
CUGBP Elav-like family member 4, transcript variant X18
CUGBP Elav-like family member 4, transcript variant X1
CUGBP Elav-like family member 4, transcript variant X5
CUGBP Elav-like family member 4, transcript variant X8
CUGBP Elav-like family member 4, transcript variant X29
CUGBP Elav-like family member 4, transcript variant X4
CUGBP Elav-like family member 4, transcript variant X19
CUGBP Elav-like family member 4, transcript variant X20
CUGBP Elav-like family member 4, transcript variant X24
CUGBP Elav-like family member 4, transcript variant X23
CUGBP Elav-like family member 4, transcript variant X28
CUGBP Elav-like family member 4, transcript variant X6
CUGBP Elav-like family member 4 isoform X1
CUGBP Elav-like family member 4 isoform X12
CUGBP Elav-like family member 4 isoform X16
CUGBP Elav-like family member 4 isoform X30
CUGBP Elav-like family member 4 isoform X6
CUGBP Elav-like family member 4 isoform X26
CUGBP Elav-like family member 4 isoform X2
CUGBP Elav-like family member 4 isoform X4
CUGBP Elav-like family member 4 isoform X32
CUGBP Elav-like family member 4 isoform X18
CUGBP Elav-like family member 4 isoform X5
CUGBP Elav-like family member 4 isoform X17
CUGBP Elav-like family member 4 isoform X21
CUGBP Elav-like family member 4 isoform X8
CUGBP Elav-like family member 4 isoform X22
CUGBP Elav-like family member 4 isoform X25
CUGBP Elav-like family member 4 isoform X10
CUGBP Elav-like family member 4 isoform X13
CUGBP Elav-like family member 4 isoform X28
CUGBP Elav-like family member 4 isoform X15
CUGBP Elav-like family member 4 isoform X20
CUGBP Elav-like family member 4 isoform X31
uncharacterized LOC123512470, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123512470, 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 10 samples with support for all annotated introns
uncharacterized protein LOC123512470 isoform X2
uncharacterized protein LOC123512470 isoform X1
CUGBP Elav-like family member 4, transcript variant X25
CUGBP Elav-like family member 4, transcript variant X26
CUGBP Elav-like family member 4 isoform X23
uncharacterized LOC123512471, transcript variant X4
uncharacterized LOC123512471, transcript variant X2
uncharacterized LOC123512471, transcript variant X3
uncharacterized LOC123512471, transcript variant X1
uncharacterized LOC123512471, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
chitinase domain-containing protein 1-like
RWD domain-containing protein 2A-like, transcript variant X1
RWD domain-containing protein 2A-like, transcript variant X4
RWD domain-containing protein 2A-like, transcript variant X3
RWD domain-containing protein 2A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 17 samples with support for all annotated introns
uncharacterized LOC123512269, 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 9 samples with support for all annotated introns
uncharacterized LOC123512269, 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 12 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 5 samples with support for all annotated introns
BMP-binding endothelial regulator protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
BMP-binding endothelial regulator protein-like, transcript variant X4
BMP-binding endothelial regulator protein-like, transcript variant X1
BMP-binding endothelial regulator protein-like, transcript variant X2
BMP-binding endothelial regulator protein-like
ras-related protein Rab6, transcript variant X2
ras-related protein Rab6, transcript variant X1
pollen-specific leucine-rich repeat extensin-like protein 3
suppressor of lurcher protein 1-like, transcript variant X2
suppressor of lurcher protein 1-like, transcript variant X1
suppressor of lurcher protein 1-like isoform X1
suppressor of lurcher protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123512252, transcript variant X1
uncharacterized LOC123512252, 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 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: 77% coverage of the annotated genomic feature by RNAseq alignments
KH domain-containing protein akap-1-like, transcript variant X1
KH domain-containing protein akap-1-like, transcript variant X3
KH domain-containing protein akap-1-like, transcript variant X2
KH domain-containing protein akap-1-like isoform X1
KH domain-containing protein akap-1-like isoform X3
KH domain-containing protein akap-1-like isoform X2
collagen alpha-1(III) chain-like, transcript variant X6
collagen alpha-1(III) chain-like, transcript variant X1
collagen alpha-1(III) chain-like, transcript variant X2
collagen alpha-1(III) chain-like, transcript variant X5
collagen alpha-1(I) chain-like isoform X1
collagen alpha-1(I) chain-like isoform X2
collagen alpha-1(XXVII) chain-like isoform X4
collagen alpha-1(III) chain-like isoform X5
collagen alpha-1(III) chain-like, transcript variant X3
collagen alpha-1(III) chain-like, transcript variant X4
collagen alpha-1(I) chain-like isoform X3
probable ubiquitin carboxyl-terminal hydrolase MINDY-4
uncharacterized LOC123512255, transcript variant X4
uncharacterized LOC123512255, transcript variant X5
uncharacterized LOC123512255, transcript variant X2
uncharacterized protein LOC123512255 isoform X2
uncharacterized LOC123512255, transcript variant X1
uncharacterized LOC123512255, transcript variant X3
uncharacterized protein LOC123512255 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 4 Proteins, and 100% 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: allatostatin-A receptor-like
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
neuronal acetylcholine receptor subunit alpha-10-like
macrophage mannose receptor 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
macrophage mannose receptor 1-like, transcript variant X1
transfer RNA proline (anticodon AGG); 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: 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
death-inducer obliterator 1-like, transcript variant X1
death-inducer obliterator 1-like, transcript variant X3
death-inducer obliterator 1-like, transcript variant X2
death-inducer obliterator 1-like, transcript variant X5
death-inducer obliterator 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
death-inducer obliterator 1-like isoform X1
death-inducer obliterator 1-like isoform X3
death-inducer obliterator 1-like isoform X2
death-inducer obliterator 1-like isoform X4
death-inducer obliterator 1-like isoform X5
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X1
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X2
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X5
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X16
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X17
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X7
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X8
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X12
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X31
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X6
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X10
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X14
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X25
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X18
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X27
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X20
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X28
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X21
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X23
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X4
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X3
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X9
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X13
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X11
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X15
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X19
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X26
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X22
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X24
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X29
E3 ubiquitin-protein ligase SH3RF1-like, transcript variant X30
E3 ubiquitin-protein ligase SH3RF1-like isoform X1
E3 ubiquitin-protein ligase SH3RF1-like isoform X8
E3 ubiquitin-protein ligase SH3RF1-like isoform X3
E3 ubiquitin-protein ligase SH3RF1-like isoform X4
E3 ubiquitin-protein ligase SH3RF1-like isoform X9
E3 ubiquitin-protein ligase SH3RF1-like isoform X6
E3 ubiquitin-protein ligase SH3RF1-like isoform X11
E3 ubiquitin-protein ligase SH3RF1-like isoform X13
E3 ubiquitin-protein ligase SH3RF1-like isoform X2
E3 ubiquitin-protein ligase SH3RF1-like isoform X5
E3 ubiquitin-protein ligase SH3RF1-like isoform X10
E3 ubiquitin-protein ligase SH3RF1-like isoform X7
E3 ubiquitin-protein ligase SH3RF1-like isoform X12
collagen alpha-2(IX) chain-like, transcript variant X4
collagen alpha-2(IX) chain-like, transcript variant X5
collagen alpha-2(IX) chain-like, transcript variant X3
collagen alpha-2(IX) chain-like, transcript variant X1
collagen alpha-2(IX) chain-like, transcript variant X2
collagen alpha-2(IX) chain-like isoform X4
collagen alpha-1(I) chain-like isoform X5
collagen alpha-2(IX) chain-like isoform X3
collagen alpha-2(IX) chain-like 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
procollagen-lysine,2-oxoglutarate 5-dioxygenase 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: procollagen-lysine,2-oxoglutarate 5-dioxygenase 1-like
phospholipid-transporting ATPase ABCA3-like, transcript variant X2
phospholipid-transporting ATPase ABCA3-like, transcript variant X3
phospholipid-transporting ATPase ABCA3-like, transcript variant X1
phospholipid-transporting ATPase ABCA3-like isoform X1
phospholipid-transporting ATPase ABCA3-like isoform X2
uncharacterized LOC123512356, transcript variant X2
uncharacterized LOC123512356, transcript variant X1
uncharacterized protein LOC123512356 isoform X1
uncharacterized protein LOC123512356 isoform X2
uncharacterized LOC123512328, transcript variant X1
uncharacterized LOC123512328, transcript variant X3
uncharacterized LOC123512328, transcript variant X2
EH domain-containing protein 3-like, transcript variant X1
EH domain-containing protein 3-like, transcript variant X2
EH domain-containing protein 3-like isoform X1
EH domain-containing protein 3-like isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
pollen-specific leucine-rich repeat extensin-like protein 1, transcript variant X2
pollen-specific leucine-rich repeat extensin-like protein 1, transcript variant X1
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X2
pollen-specific leucine-rich repeat extensin-like protein 1 isoform X1
oxidized low-density lipoprotein receptor 1-like
2-oxoglutarate-Fe(II) type oxidoreductase ppzD-like
glucose-induced degradation protein 4 homolog
glutamate receptor ionotropic, delta-1-like, transcript variant X1
glutamate receptor ionotropic, delta-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, delta-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 91% 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC123512195
uncharacterized LOC123512415, transcript variant X1
uncharacterized LOC123512415, transcript variant X2
uncharacterized LOC123512159, transcript variant X1
uncharacterized LOC123512159, transcript variant X2
electron transfer flavoprotein subunit alpha, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
putative nuclease HARBI1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
putative nuclease HARBI1, 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
venom metalloproteinase antarease-like TtrivMP_A
uncharacterized LOC123512171, transcript variant X4
uncharacterized LOC123512171, transcript variant X2
uncharacterized LOC123512171, transcript variant X3
uncharacterized LOC123512171, transcript variant X6
uncharacterized LOC123512171, transcript variant X5
uncharacterized LOC123512171, transcript variant X1
uncharacterized protein LOC123512171 isoform X2
uncharacterized protein LOC123512171 isoform X3
uncharacterized protein LOC123512171 isoform X1
uncharacterized LOC123512171, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC123512171, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized protein LOC123512171 isoform X4
uncharacterized LOC123512171, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC123512171, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein LOC123512171 isoform X5
vacuolar protein sorting-associated protein 35-like
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
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
transfer RNA valine (anticodon GAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 43% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA leucine (anticodon AAG); 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: 86% 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: 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
calcium/calmodulin-dependent protein kinase type 1, transcript variant X4
calcium/calmodulin-dependent protein kinase type 1, transcript variant X3
calcium/calmodulin-dependent protein kinase type 1 isoform X4
calcium/calmodulin-dependent protein kinase type 1 isoform X3
calcium/calmodulin-dependent protein kinase type 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
calcium/calmodulin-dependent protein kinase type 1 isoform X2
calcium/calmodulin-dependent protein kinase type 1 isoform X1
uncharacterized LOC123512179, transcript variant X3
uncharacterized LOC123512179, transcript variant X2
uncharacterized LOC123512179, transcript variant X1
uncharacterized protein LOC123512179 isoform X3
uncharacterized protein LOC123512179 isoform X2
uncharacterized protein LOC123512179 isoform X1
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nipped-B-like protein, transcript variant X3
nipped-B-like protein, transcript variant X1
nipped-B-like protein, transcript variant X2
transfer RNA glycine (anticodon CCC); 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.
G patch domain-containing protein 1-like, transcript variant X2
G patch domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
G patch domain-containing protein 1-like isoform X1
G patch domain-containing protein 1-like isoform X2
piggyBac transposable element-derived protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 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 72% coverage of the annotated genomic feature by RNAseq alignments
PAX3- and PAX7-binding protein 1-like, transcript variant X2
PAX3- and PAX7-binding protein 1-like, transcript variant X1
PAX3- and PAX7-binding protein 1-like isoform X2
PAX3- and PAX7-binding protein 1-like isoform X1
uncharacterized LOC123512438, transcript variant X2
uncharacterized LOC123512438, transcript variant X1
uncharacterized LOC123512438, 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 3 samples with support for all annotated introns
uncharacterized LOC123512438, transcript variant X3
uncharacterized LOC123512438, transcript variant X5
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon CGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized mitochondrial protein AtMg00860-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
sodium/potassium-transporting ATPase subunit beta-2-like
dimethylglycine dehydrogenase, mitochondrial-like, transcript variant X2
dimethylglycine dehydrogenase, mitochondrial-like, transcript variant X1
dimethylglycine dehydrogenase, mitochondrial-like isoform X1
dimethylglycine dehydrogenase, mitochondrial-like isoform X2
betaine--homocysteine S-methyltransferase 1-like
glutamate receptor ionotropic, kainate 5-like
eukaryotic translation initiation factor 4E type 2-like, transcript variant X2
eukaryotic translation initiation factor 4E type 2-like, transcript variant X3
eukaryotic translation initiation factor 4E type 2-like isoform X2
eukaryotic translation initiation factor 4E type 2-like, transcript variant X1
eukaryotic translation initiation factor 4E type 2-like, transcript variant X4
eukaryotic translation initiation factor 4E type 2-like isoform X3
eukaryotic translation initiation factor 4E type 2-like isoform 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
N-lysine methyltransferase KMT5A-A-like, transcript variant X2
N-lysine methyltransferase KMT5A-A-like, transcript variant X3
N-lysine methyltransferase KMT5A-A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
golgin subfamily A member 6-like protein 22
vicilin-like seed storage protein At2g18540, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
vicilin-like seed storage protein At2g18540, transcript variant X1
vicilin-like seed storage protein At2g18540, transcript variant X2
vicilin-like seed storage protein At2g18540 isoform X2
vicilin-like seed storage protein At2g18540 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123512457, 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 37 samples with support for all annotated introns
uncharacterized LOC123512457, transcript variant X2
uncharacterized LOC123512457, 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 41 samples with support for all annotated introns
uncharacterized protein LOC123512457 isoform X1
uncharacterized protein LOC123512457 isoform X2
uncharacterized protein LOC123512457 isoform X3
uncharacterized LOC123512458, transcript variant X2
uncharacterized protein LOC123512458 isoform X2
uncharacterized LOC123512458, transcript variant X3
uncharacterized LOC123512458, transcript variant X1
uncharacterized protein LOC123512458 isoform X1
uncharacterized protein LOC123512458 isoform X3
mitochondrial inner membrane protease subunit 1-like, transcript variant X1
mitochondrial inner membrane protease subunit 1-like, transcript variant X3
mitochondrial inner membrane protease subunit 1-like, transcript variant X2
mitochondrial inner membrane protease subunit 1-like isoform X1
mitochondrial inner membrane protease subunit 1-like isoform X3
mitochondrial inner membrane protease subunit 1-like isoform X2
mitotic checkpoint protein BUB3-like, transcript variant X4
mitotic checkpoint protein BUB3-like, transcript variant X1
mitotic checkpoint protein BUB3-like, transcript variant X3
mitotic checkpoint protein BUB3-like, transcript variant X2
mitotic checkpoint protein BUB3-like isoform X1
mitotic checkpoint protein BUB3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
aminopeptidase NAALADL1-like, transcript variant X1
aminopeptidase NAALADL1-like, transcript variant X4
aminopeptidase NAALADL1-like, transcript variant X5
aminopeptidase NAALADL1-like, transcript variant X2
aminopeptidase NAALADL1-like, transcript variant X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1 homolog, transcript variant X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1 homolog, transcript variant X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1 homolog, transcript variant X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1 homolog isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1 homolog isoform X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A containing DEAD/H box 1 homolog isoform X2
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: 2 long SRA reads, 1 Protein, 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: forkhead box protein O3-like
cell adhesion molecule 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cell adhesion molecule 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
cell adhesion molecule 1-like, transcript variant X2
cell adhesion molecule 1-like isoform X2
cell adhesion molecule 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
uncharacterized LOC123512208, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123512208, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
uncharacterized protein LOC123512208 isoform X1
uncharacterized LOC123512208, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein LOC123512208 isoform X2
FAST kinase domain-containing protein 4-like, transcript variant X2
FAST kinase domain-containing protein 4-like, transcript variant X1
FAST kinase domain-containing protein 4-like isoform X2
FAST kinase domain-containing protein 4-like isoform X1
U3 small nucleolar RNA-associated protein 15 homolog
recombining binding protein suppressor of hairless-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
LOW QUALITY PROTEIN: recombining binding protein suppressor of hairless-like
PRKCA-binding protein-like, transcript variant X5
PRKCA-binding protein-like, transcript variant X1
PRKCA-binding protein-like, transcript variant X3
PRKCA-binding protein-like, transcript variant X2
PRKCA-binding protein-like, transcript variant X4
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
PRKCA-binding protein-like, transcript variant X6
PRKCA-binding protein-like, transcript variant X7
protein N-terminal asparagine amidohydrolase-like, transcript variant X2
protein N-terminal asparagine amidohydrolase-like, transcript variant X1
protein N-terminal asparagine amidohydrolase-like
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
proteoglycan 4-like, transcript variant X1
proteoglycan 4-like, transcript variant X2
probable nuclear transport factor 2, transcript variant X2
probable nuclear transport factor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
LOW QUALITY PROTEIN: exocyst complex component 2-like
MBT domain-containing protein 1-like, transcript variant X7
MBT domain-containing protein 1-like, transcript variant X4
MBT domain-containing protein 1-like, transcript variant X3
MBT domain-containing protein 1-like, transcript variant X6
MBT domain-containing protein 1-like, transcript variant X2
MBT domain-containing protein 1-like, transcript variant X5
MBT domain-containing protein 1-like, transcript variant X1
MBT domain-containing protein 1-like isoform X7
MBT domain-containing protein 1-like isoform X4
MBT domain-containing protein 1-like isoform X3
MBT domain-containing protein 1-like isoform X6
lethal(3)malignant brain tumor-like protein 2 isoform X2
MBT domain-containing protein 1-like isoform X5
lethal(3)malignant brain tumor-like protein 2 isoform X1
Y' element ATP-dependent helicase YEL077C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 76% coverage of the annotated genomic feature by RNAseq alignments
ras-related and estrogen-regulated growth inhibitor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor-like isoform X1
ras-related and estrogen-regulated growth inhibitor-like isoform X2
myotubularin-related protein 4-like, transcript variant X8
myotubularin-related protein 4-like, transcript variant X11
myotubularin-related protein 4-like, transcript variant X4
myotubularin-related protein 4-like, transcript variant X7
myotubularin-related protein 4-like, transcript variant X3
myotubularin-related protein 4-like, transcript variant X6
myotubularin-related protein 4-like, transcript variant X2
myotubularin-related protein 4-like, transcript variant X5
myotubularin-related protein 4-like, transcript variant X1
myotubularin-related protein 4-like isoform X8
myotubularin-related protein 3-like isoform X4
myotubularin-related protein 4-like isoform X7
myotubularin-related protein 3-like isoform X3
myotubularin-related protein 4-like isoform X6
myotubularin-related protein 3-like isoform X2
myotubularin-related protein 4-like isoform X5
myotubularin-related protein 3-like isoform X1
myotubularin-related protein 4-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
myotubularin-related protein 4-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
myotubularin-related protein 3-like isoform X11
myotubularin-related protein 4-like isoform X10
myotubularin-related protein 4-like isoform X9
TBC1 domain family member 14-like, transcript variant X2
TBC1 domain family member 14-like, transcript variant X1
TBC1 domain family member 14-like isoform X2
TBC1 domain family member 14-like isoform X1
lipid droplet-regulating VLDL assembly factor AUP1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 66% 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 long SRA reads, 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: 1 long SRA read, 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC123512225, transcript variant X2
uncharacterized LOC123512225, transcript variant X1
uncharacterized protein LOC123512225 isoform X2
uncharacterized protein LOC123512225 isoform X1
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC123512331, transcript variant X2
uncharacterized LOC123512331, transcript variant X1
uncharacterized LOC123512331, transcript variant X4
uncharacterized LOC123512331, transcript variant X3
zinc finger BED domain-containing protein 5-like
carboxypeptidase N subunit 2-like, transcript variant X2
carboxypeptidase N subunit 2-like, transcript variant X1
carboxypeptidase N subunit 2-like, transcript variant X3
serine/arginine repetitive matrix protein 2-like, transcript variant X3
serine/arginine repetitive matrix protein 2-like, transcript variant X2
serine/arginine repetitive matrix protein 2-like, transcript variant X1
serine/arginine repetitive matrix protein 2-like isoform X1
serine/arginine repetitive matrix protein 2-like isoform X2
splicing factor ESS-2 homolog, transcript variant X2
splicing factor ESS-2 homolog, transcript variant X1
inter-alpha-trypsin inhibitor heavy chain H5-like
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
LOW QUALITY PROTEIN: inter-alpha-trypsin inhibitor heavy chain H5-like
oxytocin receptor-like, transcript variant X1
oxytocin receptor-like, transcript variant X2
C3 and PZP-like alpha-2-macroglobulin domain-containing protein 8
lon protease homolog 2, peroxisomal-like
LOW QUALITY PROTEIN: lon protease homolog 2, peroxisomal-like
signal recognition particle 9 kDa protein-like
E3 ubiquitin-protein ligase NRDP1-like, transcript variant X2
E3 ubiquitin-protein ligase NRDP1-like, transcript variant X1
E3 ubiquitin-protein ligase NRDP1-like, transcript variant X3
E3 ubiquitin-protein ligase NRDP1-like, transcript variant X5
E3 ubiquitin-protein ligase NRDP1-like, transcript variant X6
E3 ubiquitin-protein ligase NRDP1-like, transcript variant X8
E3 ubiquitin-protein ligase NRDP1-like, transcript variant X4
E3 ubiquitin-protein ligase NRDP1-like, transcript variant X7
E3 ubiquitin-protein ligase NRDP1-like, transcript variant X9
E3 ubiquitin-protein ligase NRDP1-like, transcript variant X10
E3 ubiquitin-protein ligase NRDP1-like isoform X1
E3 ubiquitin-protein ligase NRDP1-like isoform X2
E3 ubiquitin-protein ligase NRDP1-like isoform X4
E3 ubiquitin-protein ligase NRDP1-like isoform X6
E3 ubiquitin-protein ligase NRDP1-like isoform X3
E3 ubiquitin-protein ligase NRDP1-like isoform X5
E3 ubiquitin-protein ligase NRDP1-like isoform X7
E3 ubiquitin-protein ligase NRDP1-like isoform X8
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: uncharacterized protein LOC123512312
protein glass-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein glass-like, transcript variant X2
protein glass-like, transcript variant X1
protein glass-like, 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
leucine-rich repeat extensin-like protein 5 isoform X2
transcription factor Sp8-like isoform X1
dipeptidyl peptidase 1-like, transcript variant X3
dipeptidyl peptidase 1-like, transcript variant X1
dipeptidyl peptidase 1-like, transcript variant X2
dipeptidyl peptidase 1-like, transcript variant X4
WW domain-binding protein 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
WW domain-binding protein 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
WW domain-binding protein 4-like isoform X1
WW domain-binding protein 4-like isoform X2
peroxisomal acyl-coenzyme A oxidase 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
peroxisomal acyl-coenzyme A oxidase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
peroxisomal acyl-coenzyme A oxidase 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
peroxisomal acyl-coenzyme A oxidase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
peroxisomal acyl-coenzyme A oxidase 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
peroxisomal acyl-coenzyme A oxidase 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
peroxisomal acyl-coenzyme A oxidase 1-like
coenzyme Q-binding protein COQ10 homolog B, mitochondrial-like
sulfotransferase 1A1-like, transcript variant X2
sulfotransferase 1A1-like, transcript variant X1
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like, transcript variant X2
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like, transcript variant X1
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like isoform X2
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like isoform X1
transforming growth factor-beta-induced protein ig-h3-like
LOW QUALITY PROTEIN: transforming growth factor-beta-induced protein ig-h3-like
proprotein convertase subtilisin/kexin type 4-like
protein obstructor-E-like, transcript variant X3
protein obstructor-E-like, transcript variant X2
protein obstructor-E-like, transcript variant X4
protein obstructor-E-like, transcript variant X1
uncharacterized LOC123512359, transcript variant X1
uncharacterized LOC123512359, transcript variant X2
uncharacterized protein LOC123512359 isoform X1
uncharacterized protein LOC123512359 isoform X2
protein farnesyltransferase subunit beta-like, transcript variant X5
protein farnesyltransferase subunit beta-like, transcript variant X2
protein farnesyltransferase subunit beta-like, transcript variant X4
protein farnesyltransferase subunit beta-like, transcript variant X1
protein farnesyltransferase subunit beta-like, transcript variant X3
protein farnesyltransferase subunit beta-like isoform X2
protein farnesyltransferase subunit beta-like isoform X4
protein farnesyltransferase subunit beta-like isoform X1
protein farnesyltransferase subunit beta-like isoform X3
protein farnesyltransferase subunit beta-like isoform X5
uncharacterized LOC123512363, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC123512363, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
intracellular coagulation inhibitor 1-like
intracellular coagulation inhibitor 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
intracellular coagulation inhibitor 1-like, transcript variant X5
intracellular coagulation inhibitor 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
intracellular coagulation inhibitor 1-like, transcript variant X4
intracellular coagulation inhibitor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
intracellular coagulation inhibitor 1-like, transcript variant X2
intracellular coagulation inhibitor 1-like isoform X1
long-chain-fatty-acid--CoA ligase 4-like, transcript variant X1
long-chain-fatty-acid--CoA ligase 4-like, transcript variant X2
long-chain-fatty-acid--CoA ligase 4-like
mediator of RNA polymerase II transcription subunit 28-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
baculoviral IAP repeat-containing protein 5-like, transcript variant X2
baculoviral IAP repeat-containing protein 5-like, transcript variant X1
baculoviral IAP repeat-containing protein 5-like isoform X1
baculoviral IAP repeat-containing protein 5-like isoform X2
ATP-dependent translocase ABCB1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like isoform X1
ATP-dependent translocase ABCB1-like isoform X2
ATP-dependent translocase ABCB1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ATP-dependent translocase ABCB1-like isoform X3
60S ribosomal protein L29-1-like, transcript variant X1
60S ribosomal protein L29-1-like, transcript variant X2
serine palmitoyltransferase 2-like, transcript variant X4
serine palmitoyltransferase 2-like isoform X4
serine palmitoyltransferase 2-like, transcript variant X2
serine palmitoyltransferase 2-like, transcript variant X7
serine palmitoyltransferase 2-like, transcript variant X6
serine palmitoyltransferase 2-like, transcript variant X1
serine palmitoyltransferase 2-like, transcript variant X5
serine palmitoyltransferase 2-like isoform X2
serine palmitoyltransferase 2-like isoform X1
serine palmitoyltransferase 2-like isoform X6
serine palmitoyltransferase 2-like, transcript variant X3
serine palmitoyltransferase 2-like isoform X3
serine palmitoyltransferase 2-like isoform X5
uncharacterized LOC123512377, transcript variant X3
uncharacterized LOC123512377, transcript variant X2
uncharacterized LOC123512377, transcript variant X1
uncharacterized LOC123512377, 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 5 samples with support for all annotated introns
tudor domain-containing protein 7-like, transcript variant X2
tudor domain-containing protein 7-like, transcript variant X1
tudor domain-containing protein 7-like, transcript variant X3
tudor domain-containing protein 7-like isoform X1
tudor domain-containing protein 7-like isoform X2
uncharacterized LOC123512389, transcript variant X3
uncharacterized LOC123512389, 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 7 samples with support for all annotated introns
uncharacterized LOC123512389, 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
mastermind-like domain-containing protein 1
LOW QUALITY PROTEIN: delta(7)-sterol 5(6)-desaturase-like
dorsal-ventral patterning protein Sog-like
LOW QUALITY PROTEIN: dorsal-ventral patterning protein Sog-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
cell division cycle and apoptosis regulator protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
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: cell division cycle and apoptosis regulator protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
active regulator of SIRT1-like, transcript variant X2
active regulator of SIRT1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
SH3 and multiple ankyrin repeat domains protein 3-like
LOW QUALITY PROTEIN: SH3 and multiple ankyrin repeat domains protein 3-like
insulin-like growth factor 2 mRNA-binding protein 1, transcript variant X2
insulin-like growth factor 2 mRNA-binding protein 1, transcript variant X1
insulin-like growth factor 2 mRNA-binding protein 1 isoform X1
insulin-like growth factor 2 mRNA-binding protein 1 isoform X2
insulin-like growth factor 2 mRNA-binding protein 1, transcript variant X5
insulin-like growth factor 2 mRNA-binding protein 1, transcript variant X4
insulin-like growth factor 2 mRNA-binding protein 1 isoform X4
insulin-like growth factor 2 mRNA-binding protein 1 isoform X5
insulin-like growth factor 2 mRNA-binding protein 1, transcript variant X3
insulin-like growth factor 2 mRNA-binding protein 1 isoform X3
insulin-like growth factor 2 mRNA-binding protein 1, transcript variant X6
insulin-like growth factor 2 mRNA-binding protein 1 isoform X6
pre-mRNA-splicing factor CWC22 homolog, transcript variant X1
pre-mRNA-splicing factor CWC22 homolog isoform X1
pre-mRNA-splicing factor CWC22 homolog, transcript variant X3
pre-mRNA-splicing factor CWC22 homolog, transcript variant X2
pre-mRNA-splicing factor CWC22 homolog isoform X2
LOW QUALITY PROTEIN: uncharacterized protein LOC123512334
serine/threonine-protein phosphatase 6 catalytic subunit-like, transcript variant X2
serine/threonine-protein phosphatase 6 catalytic subunit-like, transcript variant X1
serine/threonine-protein phosphatase 6 catalytic subunit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
sodium bicarbonate transporter-like protein 11, transcript variant X8
sodium bicarbonate transporter-like protein 11, transcript variant X1
sodium bicarbonate transporter-like protein 11, transcript variant X3
sodium bicarbonate transporter-like protein 11, transcript variant X6
sodium bicarbonate transporter-like protein 11, transcript variant X5
sodium bicarbonate transporter-like protein 11, transcript variant X4
sodium bicarbonate transporter-like protein 11, transcript variant X2
sodium bicarbonate transporter-like protein 11, transcript variant X7
sodium bicarbonate transporter-like protein 11 isoform X3
sodium bicarbonate transporter-like protein 11 isoform X1
sodium bicarbonate transporter-like protein 11 isoform X2
UTP--glucose-1-phosphate uridylyltransferase-like, transcript variant X4
UTP--glucose-1-phosphate uridylyltransferase-like, transcript variant X5
UTP--glucose-1-phosphate uridylyltransferase-like, transcript variant X2
UTP--glucose-1-phosphate uridylyltransferase-like, transcript variant X3
UTP--glucose-1-phosphate uridylyltransferase-like, transcript variant X1
UTP--glucose-1-phosphate uridylyltransferase-like isoform X4
UTP--glucose-1-phosphate uridylyltransferase-like isoform X3
UTP--glucose-1-phosphate uridylyltransferase-like isoform X2
UTP--glucose-1-phosphate uridylyltransferase-like isoform X1
UTP--glucose-1-phosphate uridylyltransferase-like isoform X5
C2 domain-containing protein 5-like, transcript variant X7
C2 domain-containing protein 5-like, transcript variant X6
C2 domain-containing protein 5-like, transcript variant X5
C2 domain-containing protein 5-like, transcript variant X4
C2 domain-containing protein 5-like, transcript variant X3
C2 domain-containing protein 5-like, transcript variant X2
C2 domain-containing protein 5-like, transcript variant X1
C2 domain-containing protein 5-like isoform X7
C2 domain-containing protein 5-like isoform X6
C2 domain-containing protein 5-like isoform X5
C2 domain-containing protein 5-like isoform X4
C2 domain-containing protein 5-like isoform X3
C2 domain-containing protein 5-like isoform X2
C2 domain-containing protein 5-like isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: nodal modulator 1-like
protein FAM92A-like, transcript variant X1
protein FAM92A-like, transcript variant X2
DNA-directed RNA polymerase II subunit RPB7
39S ribosomal protein L47, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
irregular chiasm C-roughest protein-like, transcript variant X2
irregular chiasm C-roughest protein-like, transcript variant X1
irregular chiasm C-roughest protein-like isoform X1
irregular chiasm C-roughest protein-like isoform X2
tetratricopeptide repeat protein 28-like
LOW QUALITY PROTEIN: tetratricopeptide repeat protein 28-like
5-aminolevulinate synthase, erythroid-specific, mitochondrial-like, transcript variant X3
5-aminolevulinate synthase, erythroid-specific, mitochondrial-like, transcript variant X1
5-aminolevulinate synthase, erythroid-specific, mitochondrial-like, transcript variant X4
5-aminolevulinate synthase, erythroid-specific, mitochondrial-like isoform X1
5-aminolevulinate synthase, erythroid-specific, mitochondrial-like isoform X3
5-aminolevulinate synthase, erythroid-specific, mitochondrial-like, transcript variant X2
5-aminolevulinate synthase, erythroid-specific, mitochondrial-like, transcript variant X5
5-aminolevulinate synthase, erythroid-specific, mitochondrial-like isoform X2
5-aminolevulinate synthase, erythroid-specific, mitochondrial-like isoform X4
uncharacterized LOC123512244, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC123512244, transcript variant X1
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like
LOW QUALITY PROTEIN: tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like
leucine-zipper-like transcriptional regulator 1, transcript variant X3
leucine-zipper-like transcriptional regulator 1, transcript variant X4
leucine-zipper-like transcriptional regulator 1, transcript variant X2
leucine-zipper-like transcriptional regulator 1, transcript variant X1
leucine-zipper-like transcriptional regulator 1 isoform X1
leucine-zipper-like transcriptional regulator 1 isoform X2
putative mediator of RNA polymerase II transcription subunit 17, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 17, transcript variant X3
putative mediator of RNA polymerase II transcription subunit 17, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
putative mediator of RNA polymerase II transcription subunit 17
LOW QUALITY PROTEIN: laminin subunit beta-1-like
bifunctional glutamate/proline--tRNA ligase-like
dentin sialophosphoprotein-like, transcript variant X2
dentin sialophosphoprotein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc metalloproteinase nas-14-like, transcript variant X1
zinc metalloproteinase nas-14-like, transcript variant X2
zinc metalloproteinase nas-14-like isoform X1
zinc metalloproteinase nas-4-like isoform X2
LOW QUALITY PROTEIN: uncharacterized protein LOC123512321
alpha-1,6-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X5
alpha-1,6-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X3
alpha-1,6-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X2
alpha-1,6-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X1
alpha-1,6-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like, transcript variant X4
alpha-1,6-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like isoform X1
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C-like isoform X3
alpha-1,6-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase-like isoform X2
charged multivesicular body protein 4c-like, transcript variant X1
charged multivesicular body protein 4c-like, transcript variant X2
charged multivesicular body protein 4c-like
uncharacterized LOC123512276, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC123512276 isoform X1
uncharacterized LOC123512276, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized protein LOC123512276 isoform X2