ENST00000695651.1:n.963T>A
|
|
|
ENST00000695652.1:c.2492T>A
|
ENSP00000512083.1:p.Phe831Tyr
|
|
ENST00000695653.1:c.524T>A
|
ENSP00000512084.1:p.Phe175Tyr
|
|
ENST00000695654.1:c.1739T>A
|
ENSP00000512085.1:p.Phe580Tyr
|
|
ENST00000695655.1:c.1556T>A
|
ENSP00000512086.1:n.1556T>A
|
|
ENST00000695692.1:n.1979T>A
|
|
|
ENST00000245907.11:c.2615T>A
MANE Select
|
ENSP00000245907.4:p.Phe872Tyr
|
|
ENST00000245907.10:c.2615T>A
|
ENSP00000245907.4:p.Phe872Tyr
|
|
ENST00000594005.1:n.191T>A
|
|
|
NM_000064.3:c.2615T>A
|
NP_000055.2:p.Phe872Tyr
|
|
NM_000064.4:c.2615T>A
MANE Select
|
NP_000055.2:p.Phe872Tyr
|
|