ENST00000695651.1:n.963T>G
|
|
|
ENST00000695652.1:c.2492T>G
|
ENSP00000512083.1:p.Phe831Cys
|
|
ENST00000695653.1:c.524T>G
|
ENSP00000512084.1:p.Phe175Cys
|
|
ENST00000695654.1:c.1739T>G
|
ENSP00000512085.1:p.Phe580Cys
|
|
ENST00000695655.1:c.1556T>G
|
ENSP00000512086.1:n.1556T>G
|
|
ENST00000695692.1:n.1979T>G
|
|
|
ENST00000245907.11:c.2615T>G
MANE Select
|
ENSP00000245907.4:p.Phe872Cys
|
|
ENST00000245907.10:c.2615T>G
|
ENSP00000245907.4:p.Phe872Cys
|
|
ENST00000594005.1:n.191T>G
|
|
|
NM_000064.3:c.2615T>G
|
NP_000055.2:p.Phe872Cys
|
|
NM_000064.4:c.2615T>G
MANE Select
|
NP_000055.2:p.Phe872Cys
|
|