|
NM_001080.3:c.755G>T
MANE Select
|
NP_001071.1:p.Gly252Val
|
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ENST00000357578.8:c.755G>T
MANE Select
|
ENSP00000350191.3:p.Gly252Val
|
|
NM_001368954.1:c.727-5206G>T
|
NP_001355883.1:n.727-5206G>T
|
|
NM_170740.1:c.794G>T
|
NP_733936.1:p.Gly265Val
|
|
ENST00000348925.2:c.794G>T
|
ENSP00000314649.3:p.Gly265Val
|
|
ENST00000357578.7:c.755G>T
|
ENSP00000350191.3:p.Gly252Val
|
|
ENST00000491546.5:c.671G>T
|
ENSP00000417687.1:p.Gly224Val
|
|
ENST00000672352.1:c.490-5206G>T
|
ENSP00000500876.1:n.490-5206G>T
|
|
ENST00000672557.1:c.673G>T
|
|
|
ENST00000672619.1:n.115G>T
|
|
|
ENST00000672652.1:c.718G>T
|
|
|
ENST00000675422.1:n.1515G>T
|
|