ENST00000695651.1:n.2193A>G
|
|
|
ENST00000695653.1:c.1754A>G
|
ENSP00000512084.1:p.Tyr585Cys
|
|
ENST00000695654.1:c.2870A>G
|
ENSP00000512085.1:p.Tyr957Cys
|
|
ENST00000695690.1:n.36A>G
|
|
|
ENST00000695691.1:n.36A>G
|
|
|
ENST00000245907.11:c.3845A>G
MANE Select
|
ENSP00000245907.4:p.Tyr1282Cys
|
|
ENST00000245907.10:c.3845A>G
|
ENSP00000245907.4:p.Tyr1282Cys
|
|
ENST00000596238.1:n.288A>G
|
|
|
ENST00000601008.1:c.241+1634A>G
|
ENSP00000471384.1:n.241+1634A>G
|
|
NM_000064.3:c.3845A>G
|
NP_000055.2:p.Tyr1282Cys
|
|
NM_000064.4:c.3845A>G
MANE Select
|
NP_000055.2:p.Tyr1282Cys
|
|