ENST00000695651.1:n.829G>A
|
|
|
ENST00000695652.1:c.2358G>A
|
ENSP00000512083.1:p.Gln786=
|
|
ENST00000695653.1:c.390G>A
|
ENSP00000512084.1:p.Gln130=
|
|
ENST00000695654.1:c.1605G>A
|
ENSP00000512085.1:p.Gln535=
|
|
ENST00000695655.1:c.1422G>A
|
ENSP00000512086.1:n.1422G>A
|
|
ENST00000695692.1:n.1845G>A
|
|
|
ENST00000245907.11:c.2481G>A
MANE Select
|
ENSP00000245907.4:p.Gln827=
|
|
ENST00000245907.10:c.2481G>A
|
ENSP00000245907.4:p.Gln827=
|
|
ENST00000602053.1:n.529G>A
|
|
|
NM_000064.3:c.2481G>A
|
NP_000055.2:p.Gln827=
|
|
NM_000064.4:c.2481G>A
MANE Select
|
NP_000055.2:p.Gln827=
|
|