ENST00000695651.1:n.1090T>C
|
|
|
ENST00000695652.1:c.2619T>C
|
ENSP00000512083.1:p.Ala873=
|
|
ENST00000695653.1:c.651T>C
|
ENSP00000512084.1:p.Ala217=
|
|
ENST00000695654.1:c.1866T>C
|
ENSP00000512085.1:p.Ala622=
|
|
ENST00000695655.1:c.1683T>C
|
ENSP00000512086.1:n.1683T>C
|
|
ENST00000695692.1:n.2106T>C
|
|
|
ENST00000245907.11:c.2742T>C
MANE Select
|
ENSP00000245907.4:p.Ala914=
|
|
ENST00000245907.10:c.2742T>C
|
ENSP00000245907.4:p.Ala914=
|
|
ENST00000594005.1:n.318T>C
|
|
|
NM_000064.3:c.2742T>C
|
NP_000055.2:p.Ala914=
|
|
NM_000064.4:c.2742T>C
MANE Select
|
NP_000055.2:p.Ala914=
|
|