ENST00000695651.1:n.982C>A
|
|
|
ENST00000695652.1:c.2511C>A
|
ENSP00000512083.1:p.Thr837=
|
|
ENST00000695653.1:c.543C>A
|
ENSP00000512084.1:p.Thr181=
|
|
ENST00000695654.1:c.1758C>A
|
ENSP00000512085.1:p.Thr586=
|
|
ENST00000695655.1:c.1575C>A
|
ENSP00000512086.1:n.1575C>A
|
|
ENST00000695692.1:n.1998C>A
|
|
|
ENST00000245907.11:c.2634C>A
MANE Select
|
ENSP00000245907.4:p.Thr878=
|
|
ENST00000245907.10:c.2634C>A
|
ENSP00000245907.4:p.Thr878=
|
|
ENST00000594005.1:n.210C>A
|
|
|
NM_000064.3:c.2634C>A
|
NP_000055.2:p.Thr878=
|
|
NM_000064.4:c.2634C>A
MANE Select
|
NP_000055.2:p.Thr878=
|
|