ENST00000368074.6:c.957G>C
MANE Select
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ENSP00000357053.1:p.Ala319=
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ENST00000556710.6:c.*1541G>C
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ENSP00000451235.2:n.*1541G>C
|
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ENST00000647676.1:c.1295G>C
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ENSP00000497162.1:n.1295G>C
|
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ENST00000326837.6:c.957G>C
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ENSP00000318227.2:p.Ala319=
|
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ENST00000368073.7:c.957G>C
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ENSP00000357052.3:p.Ala319=
|
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ENST00000368074.5:c.957G>C
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ENSP00000357053.1:p.Ala319=
|
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ENST00000461888.5:c.957G>C
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ENSP00000476407.1:p.Ala319=
|
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ENST00000466253.1:n.472G>C
|
|
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ENST00000556710.5:c.1419G>C
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ENSP00000451235.1:p.Ala473=
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NM_015726.3:c.957G>C
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NP_056541.2:p.Ala319=
|
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NR_028103.1:n.1469G>C
|
|
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NR_028104.1:n.1395G>C
|
|
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NM_015726.4:c.957G>C
MANE Select
|
NP_056541.2:p.Ala319=
|
|
NR_028103.2:n.1490G>C
|
|
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NR_028104.2:n.1416G>C
|
|
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