ENST00000695651.1:n.1120T>A
|
|
|
ENST00000695652.1:c.2649T>A
|
ENSP00000512083.1:p.Gly883=
|
|
ENST00000695653.1:c.681T>A
|
ENSP00000512084.1:p.Gly227=
|
|
ENST00000695654.1:c.1896T>A
|
ENSP00000512085.1:p.Gly632=
|
|
ENST00000695655.1:c.1713T>A
|
ENSP00000512086.1:n.1713T>A
|
|
ENST00000695692.1:n.2136T>A
|
|
|
ENST00000245907.11:c.2772T>A
MANE Select
|
ENSP00000245907.4:p.Gly924=
|
|
ENST00000245907.10:c.2772T>A
|
ENSP00000245907.4:p.Gly924=
|
|
ENST00000594005.1:n.348T>A
|
|
|
NM_000064.3:c.2772T>A
|
NP_000055.2:p.Gly924=
|
|
NM_000064.4:c.2772T>A
MANE Select
|
NP_000055.2:p.Gly924=
|
|