ENST00000430710.8:c.1980A>G
|
ENSP00000406288.3:p.Glu660=
|
|
ENST00000555935.2:c.493A>G
|
|
|
ENST00000555962.6:c.-110-3904A>G
|
ENSP00000495174.1:n.-110-3904A>G
|
|
ENST00000557364.6:c.2817A>G
|
ENSP00000451601.1:p.Glu939=
|
|
ENST00000643469.1:c.2817A>G
|
ENSP00000495070.1:p.Glu939=
|
|
ENST00000645140.1:c.2729A>G
|
|
|
ENST00000645206.1:n.1331A>G
|
|
|
ENST00000645929.1:c.1980A>G
|
ENSP00000494402.1:p.Glu660=
|
|
ENST00000646340.1:c.2823A>G
|
ENSP00000496730.1:p.Glu941=
|
|
ENST00000646647.2:c.2817A>G
MANE Select
|
ENSP00000495240.1:p.Glu939=
|
|
ENST00000399982.6:c.2817A>G
|
ENSP00000382863.2:p.Glu939=
|
|
ENST00000430710.7:c.1980A>G
|
ENSP00000406288.3:p.Glu660=
|
|
ENST00000555935.1:c.493A>G
|
|
|
ENST00000555962.5:n.151-3904A>G
|
|
|
ENST00000557364.5:c.2817A>G
|
ENSP00000451601.1:p.Glu939=
|
|
NM_001170629.1:c.2817A>G
|
NP_001164100.1:p.Glu939=
|
|
NM_020920.3:c.1980A>G
|
NP_065971.2:p.Glu660=
|
|
NM_001170629.2:c.2817A>G
MANE Select
|
NP_001164100.1:p.Glu939=
|
|
NM_020920.4:c.1980A>G
|
NP_065971.2:p.Glu660=
|
|