ENST00000695651.1:n.2106T>C
|
|
|
ENST00000695652.1:c.3635T>C
|
ENSP00000512083.1:p.Val1212Ala
|
|
ENST00000695653.1:c.1667T>C
|
ENSP00000512084.1:p.Val556Ala
|
|
ENST00000695654.1:c.2783T>C
|
ENSP00000512085.1:p.Val928Ala
|
|
ENST00000695655.1:c.2699T>C
|
ENSP00000512086.1:n.2699T>C
|
|
ENST00000695692.1:n.3122T>C
|
|
|
ENST00000245907.11:c.3758T>C
MANE Select
|
ENSP00000245907.4:p.Val1253Ala
|
|
ENST00000245907.10:c.3758T>C
|
ENSP00000245907.4:p.Val1253Ala
|
|
ENST00000596238.1:n.201T>C
|
|
|
ENST00000601008.1:c.241+570T>C
|
ENSP00000471384.1:n.241+570T>C
|
|
NM_000064.3:c.3758T>C
|
NP_000055.2:p.Val1253Ala
|
|
NM_000064.4:c.3758T>C
MANE Select
|
NP_000055.2:p.Val1253Ala
|
|