ENST00000695651.1:n.861C>G
|
|
|
ENST00000695652.1:c.2390C>G
|
ENSP00000512083.1:p.Ser797Cys
|
|
ENST00000695653.1:c.422C>G
|
ENSP00000512084.1:p.Ser141Cys
|
|
ENST00000695654.1:c.1637C>G
|
ENSP00000512085.1:p.Ser546Cys
|
|
ENST00000695655.1:c.1454C>G
|
ENSP00000512086.1:n.1454C>G
|
|
ENST00000695692.1:n.1877C>G
|
|
|
ENST00000245907.11:c.2513C>G
MANE Select
|
ENSP00000245907.4:p.Ser838Cys
|
|
ENST00000245907.10:c.2513C>G
|
ENSP00000245907.4:p.Ser838Cys
|
|
ENST00000602053.1:n.561C>G
|
|
|
NM_000064.3:c.2513C>G
|
NP_000055.2:p.Ser838Cys
|
|
NM_000064.4:c.2513C>G
MANE Select
|
NP_000055.2:p.Ser838Cys
|
|