ENST00000625662.3:c.2103T>G
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|
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ENST00000628118.2:c.1630T>G
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|
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ENST00000700551.1:c.*1427T>G
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ENSP00000515057.1:n.*1427T>G
|
|
ENST00000394196.9:c.2596T>G
MANE Select
|
ENSP00000377747.4:p.Ser866Ala
|
|
ENST00000635856.1:n.3168T>G
|
|
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ENST00000636306.1:n.156T>G
|
|
|
ENST00000636881.1:c.1967T>G
|
|
|
ENST00000637572.1:n.3340T>G
|
|
|
ENST00000394196.8:c.2596T>G
|
ENSP00000377747.4:p.Ser866Ala
|
|
ENST00000625463.1:c.136T>G
|
ENSP00000486391.1:p.Ser46Ala
|
|
ENST00000626874.2:c.2596T>G
|
ENSP00000486629.1:p.Ser866Ala
|
|
ENST00000628118.1:n.375T>G
|
|
|
NM_001271.3:c.2596T>G
|
NP_001262.3:p.Ser866Ala
|
|
NM_001271.4:c.2596T>G
MANE Select
|
NP_001262.3:p.Ser866Ala
|
|