ENST00000695651.1:n.2049C>G
|
|
|
ENST00000695652.1:c.3578C>G
|
ENSP00000512083.1:p.Ser1193Cys
|
|
ENST00000695653.1:c.1610C>G
|
ENSP00000512084.1:p.Ser537Cys
|
|
ENST00000695654.1:c.2726C>G
|
ENSP00000512085.1:p.Ser909Cys
|
|
ENST00000695655.1:c.2642C>G
|
ENSP00000512086.1:n.2642C>G
|
|
ENST00000695692.1:n.3065C>G
|
|
|
ENST00000245907.11:c.3701C>G
MANE Select
|
ENSP00000245907.4:p.Ser1234Cys
|
|
ENST00000245907.10:c.3701C>G
|
ENSP00000245907.4:p.Ser1234Cys
|
|
ENST00000596238.1:n.144C>G
|
|
|
ENST00000601008.1:c.241+513C>G
|
ENSP00000471384.1:n.241+513C>G
|
|
NM_000064.3:c.3701C>G
|
NP_000055.2:p.Ser1234Cys
|
|
NM_000064.4:c.3701C>G
MANE Select
|
NP_000055.2:p.Ser1234Cys
|
|