ENST00000695651.1:n.2089C>A
|
|
|
ENST00000695652.1:c.3618C>A
|
ENSP00000512083.1:p.Asp1206Glu
|
|
ENST00000695653.1:c.1650C>A
|
ENSP00000512084.1:p.Asp550Glu
|
|
ENST00000695654.1:c.2766C>A
|
ENSP00000512085.1:p.Asp922Glu
|
|
ENST00000695655.1:c.2682C>A
|
ENSP00000512086.1:n.2682C>A
|
|
ENST00000695692.1:n.3105C>A
|
|
|
ENST00000245907.11:c.3741C>A
MANE Select
|
ENSP00000245907.4:p.Asp1247Glu
|
|
ENST00000245907.10:c.3741C>A
|
ENSP00000245907.4:p.Asp1247Glu
|
|
ENST00000596238.1:n.184C>A
|
|
|
ENST00000601008.1:c.241+553C>A
|
ENSP00000471384.1:n.241+553C>A
|
|
NM_000064.3:c.3741C>A
|
NP_000055.2:p.Asp1247Glu
|
|
NM_000064.4:c.3741C>A
MANE Select
|
NP_000055.2:p.Asp1247Glu
|
|