ENST00000695651.1:n.2049C>A
|
|
|
ENST00000695652.1:c.3578C>A
|
ENSP00000512083.1:p.Ser1193Tyr
|
|
ENST00000695653.1:c.1610C>A
|
ENSP00000512084.1:p.Ser537Tyr
|
|
ENST00000695654.1:c.2726C>A
|
ENSP00000512085.1:p.Ser909Tyr
|
|
ENST00000695655.1:c.2642C>A
|
ENSP00000512086.1:n.2642C>A
|
|
ENST00000695692.1:n.3065C>A
|
|
|
ENST00000245907.11:c.3701C>A
MANE Select
|
ENSP00000245907.4:p.Ser1234Tyr
|
|
ENST00000245907.10:c.3701C>A
|
ENSP00000245907.4:p.Ser1234Tyr
|
|
ENST00000596238.1:n.144C>A
|
|
|
ENST00000601008.1:c.241+513C>A
|
ENSP00000471384.1:n.241+513C>A
|
|
NM_000064.3:c.3701C>A
|
NP_000055.2:p.Ser1234Tyr
|
|
NM_000064.4:c.3701C>A
MANE Select
|
NP_000055.2:p.Ser1234Tyr
|
|