ENST00000695651.1:n.1012C>T
|
|
|
ENST00000695652.1:c.2541C>T
|
ENSP00000512083.1:p.Ile847=
|
|
ENST00000695653.1:c.573C>T
|
ENSP00000512084.1:p.Ile191=
|
|
ENST00000695654.1:c.1788C>T
|
ENSP00000512085.1:p.Ile596=
|
|
ENST00000695655.1:c.1605C>T
|
ENSP00000512086.1:n.1605C>T
|
|
ENST00000695692.1:n.2028C>T
|
|
|
ENST00000245907.11:c.2664C>T
MANE Select
|
ENSP00000245907.4:p.Ile888=
|
|
ENST00000245907.10:c.2664C>T
|
ENSP00000245907.4:p.Ile888=
|
|
ENST00000594005.1:n.240C>T
|
|
|
NM_000064.3:c.2664C>T
|
NP_000055.2:p.Ile888=
|
|
NM_000064.4:c.2664C>T
MANE Select
|
NP_000055.2:p.Ile888=
|
|