ENST00000682424.1:c.1482G>T
|
ENSP00000507321.1:p.Glu494Asp
|
|
ENST00000299427.12:c.1596G>T
MANE Select
|
ENSP00000299427.6:p.Glu532Asp
|
|
ENST00000524611.2:n.635G>T
|
|
|
ENST00000524924.2:n.716G>T
|
|
|
ENST00000533371.6:c.867G>T
|
ENSP00000437066.1:p.Glu289Asp
|
|
ENST00000642892.1:c.867G>T
|
ENSP00000494165.1:p.Glu289Asp
|
|
ENST00000643342.1:c.669G>T
|
|
|
ENST00000643439.1:c.*1336G>T
|
ENSP00000495849.1:n.*1336G>T
|
|
ENST00000643479.1:n.1782G>T
|
|
|
ENST00000643516.1:c.1105G>T
|
|
|
ENST00000644218.1:c.1407G>T
|
ENSP00000493574.1:p.Glu469Asp
|
|
ENST00000644683.1:c.*1049G>T
|
ENSP00000494085.1:n.*1049G>T
|
|
ENST00000644810.1:c.1317G>T
|
ENSP00000495895.1:p.Glu439Asp
|
|
ENST00000644831.1:n.1772G>T
|
|
|
ENST00000644933.1:c.*462G>T
|
ENSP00000496133.1:n.*462G>T
|
|
ENST00000645285.1:c.*462G>T
|
ENSP00000495058.1:n.*462G>T
|
|
ENST00000645331.1:n.2801G>T
|
|
|
ENST00000645620.1:c.867G>T
|
ENSP00000493657.1:p.Glu289Asp
|
|
ENST00000646691.1:n.1483G>T
|
|
|
ENST00000646777.1:n.1929G>T
|
|
|
ENST00000647016.1:n.2076G>T
|
|
|
ENST00000647152.1:c.867G>T
|
ENSP00000495893.1:p.Glu289Asp
|
|
ENST00000647209.1:c.*1465G>T
|
ENSP00000495558.1:n.*1465G>T
|
|
ENST00000647346.1:n.2616G>T
|
|
|
ENST00000299427.10:c.1596G>T
|
ENSP00000299427.6:p.Glu532Asp
|
|
ENST00000533371.5:c.867G>T
|
ENSP00000437066.1:p.Glu289Asp
|
|
ENST00000611494.4:c.1596G>T
|
ENSP00000484546.1:p.Glu532Asp
|
|
NM_000391.3:c.1596G>T
|
NP_000382.3:p.Glu532Asp
|
|
NM_000391.4:c.1596G>T
MANE Select
|
NP_000382.3:p.Glu532Asp
|
|