ENST00000215882.10:c.788G>T
MANE Select
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ENSP00000215882.5:p.Gly263Val
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ENST00000215882.9:c.788G>T
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ENSP00000215882.5:p.Gly263Val
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ENST00000451283.5:c.479G>T
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ENSP00000401480.1:p.Gly160Val
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ENST00000470922.5:n.930G>T
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NM_001256534.1:c.809G>T
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NP_001243463.1:p.Gly270Val
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NM_001287387.1:c.479G>T
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NP_001274316.1:p.Gly160Val
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NM_005984.4:c.788G>T
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NP_005975.1:p.Gly263Val
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NR_046298.2:n.839G>T
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NM_005984.5:c.788G>T
MANE Select
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NP_005975.1:p.Gly263Val
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NM_001256534.2:c.809G>T
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NP_001243463.1:p.Gly270Val
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NM_001287387.2:c.479G>T
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NP_001274316.1:p.Gly160Val
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NR_046298.3:n.712G>T
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