ENST00000695651.1:n.1132C>T
|
|
|
ENST00000695652.1:c.2661C>T
|
ENSP00000512083.1:p.Ser887=
|
|
ENST00000695653.1:c.693C>T
|
ENSP00000512084.1:p.Ser231=
|
|
ENST00000695654.1:c.1908C>T
|
ENSP00000512085.1:p.Ser636=
|
|
ENST00000695655.1:c.1725C>T
|
ENSP00000512086.1:n.1725C>T
|
|
ENST00000695692.1:n.2148C>T
|
|
|
ENST00000245907.11:c.2784C>T
MANE Select
|
ENSP00000245907.4:p.Ser928=
|
|
ENST00000245907.10:c.2784C>T
|
ENSP00000245907.4:p.Ser928=
|
|
ENST00000594005.1:n.360C>T
|
|
|
NM_000064.3:c.2784C>T
|
NP_000055.2:p.Ser928=
|
|
NM_000064.4:c.2784C>T
MANE Select
|
NP_000055.2:p.Ser928=
|
|