ENST00000695651.1:n.860T>G
|
|
|
ENST00000695652.1:c.2389T>G
|
ENSP00000512083.1:p.Ser797Ala
|
|
ENST00000695653.1:c.421T>G
|
ENSP00000512084.1:p.Ser141Ala
|
|
ENST00000695654.1:c.1636T>G
|
ENSP00000512085.1:p.Ser546Ala
|
|
ENST00000695655.1:c.1453T>G
|
ENSP00000512086.1:n.1453T>G
|
|
ENST00000695692.1:n.1876T>G
|
|
|
ENST00000245907.11:c.2512T>G
MANE Select
|
ENSP00000245907.4:p.Ser838Ala
|
|
ENST00000245907.10:c.2512T>G
|
ENSP00000245907.4:p.Ser838Ala
|
|
ENST00000602053.1:n.560T>G
|
|
|
NM_000064.3:c.2512T>G
|
NP_000055.2:p.Ser838Ala
|
|
NM_000064.4:c.2512T>G
MANE Select
|
NP_000055.2:p.Ser838Ala
|
|