ENST00000695651.1:n.2094T>C
|
|
|
ENST00000695652.1:c.3623T>C
|
ENSP00000512083.1:p.Val1208Ala
|
|
ENST00000695653.1:c.1655T>C
|
ENSP00000512084.1:p.Val552Ala
|
|
ENST00000695654.1:c.2771T>C
|
ENSP00000512085.1:p.Val924Ala
|
|
ENST00000695655.1:c.2687T>C
|
ENSP00000512086.1:n.2687T>C
|
|
ENST00000695692.1:n.3110T>C
|
|
|
ENST00000245907.11:c.3746T>C
MANE Select
|
ENSP00000245907.4:p.Val1249Ala
|
|
ENST00000245907.10:c.3746T>C
|
ENSP00000245907.4:p.Val1249Ala
|
|
ENST00000596238.1:n.189T>C
|
|
|
ENST00000601008.1:c.241+558T>C
|
ENSP00000471384.1:n.241+558T>C
|
|
NM_000064.3:c.3746T>C
|
NP_000055.2:p.Val1249Ala
|
|
NM_000064.4:c.3746T>C
MANE Select
|
NP_000055.2:p.Val1249Ala
|
|