ENST00000695651.1:n.1036T>A
|
|
|
ENST00000695652.1:c.2565T>A
|
ENSP00000512083.1:p.Val855=
|
|
ENST00000695653.1:c.597T>A
|
ENSP00000512084.1:p.Val199=
|
|
ENST00000695654.1:c.1812T>A
|
ENSP00000512085.1:p.Val604=
|
|
ENST00000695655.1:c.1629T>A
|
ENSP00000512086.1:n.1629T>A
|
|
ENST00000695692.1:n.2052T>A
|
|
|
ENST00000245907.11:c.2688T>A
MANE Select
|
ENSP00000245907.4:p.Val896=
|
|
ENST00000245907.10:c.2688T>A
|
ENSP00000245907.4:p.Val896=
|
|
ENST00000594005.1:n.264T>A
|
|
|
NM_000064.3:c.2688T>A
|
NP_000055.2:p.Val896=
|
|
NM_000064.4:c.2688T>A
MANE Select
|
NP_000055.2:p.Val896=
|
|