ENST00000695651.1:n.2048T>G
|
|
|
ENST00000695652.1:c.3577T>G
|
ENSP00000512083.1:p.Ser1193Ala
|
|
ENST00000695653.1:c.1609T>G
|
ENSP00000512084.1:p.Ser537Ala
|
|
ENST00000695654.1:c.2725T>G
|
ENSP00000512085.1:p.Ser909Ala
|
|
ENST00000695655.1:c.2641T>G
|
ENSP00000512086.1:n.2641T>G
|
|
ENST00000695692.1:n.3064T>G
|
|
|
ENST00000245907.11:c.3700T>G
MANE Select
|
ENSP00000245907.4:p.Ser1234Ala
|
|
ENST00000245907.10:c.3700T>G
|
ENSP00000245907.4:p.Ser1234Ala
|
|
ENST00000596238.1:n.143T>G
|
|
|
ENST00000601008.1:c.241+512T>G
|
ENSP00000471384.1:n.241+512T>G
|
|
NM_000064.3:c.3700T>G
|
NP_000055.2:p.Ser1234Ala
|
|
NM_000064.4:c.3700T>G
MANE Select
|
NP_000055.2:p.Ser1234Ala
|
|