ENST00000430710.8:c.1436A>T
|
ENSP00000406288.3:p.Asp479Val
|
|
ENST00000555962.6:c.-110-6900A>T
|
ENSP00000495174.1:n.-110-6900A>T
|
|
ENST00000557364.6:c.2273A>T
|
ENSP00000451601.1:p.Asp758Val
|
|
ENST00000643469.1:c.2273A>T
|
ENSP00000495070.1:p.Asp758Val
|
|
ENST00000645140.1:c.2185A>T
|
|
|
ENST00000645206.1:n.787A>T
|
|
|
ENST00000645929.1:c.1436A>T
|
ENSP00000494402.1:p.Asp479Val
|
|
ENST00000646340.1:c.2279A>T
|
ENSP00000496730.1:p.Asp760Val
|
|
ENST00000646647.2:c.2273A>T
MANE Select
|
ENSP00000495240.1:p.Asp758Val
|
|
ENST00000399982.6:c.2273A>T
|
ENSP00000382863.2:p.Asp758Val
|
|
ENST00000430710.7:c.1436A>T
|
ENSP00000406288.3:p.Asp479Val
|
|
ENST00000554384.1:n.141A>T
|
|
|
ENST00000555962.5:n.151-6900A>T
|
|
|
ENST00000557364.5:c.2273A>T
|
ENSP00000451601.1:p.Asp758Val
|
|
NM_001170629.1:c.2273A>T
|
NP_001164100.1:p.Asp758Val
|
|
NM_020920.3:c.1436A>T
|
NP_065971.2:p.Asp479Val
|
|
NM_001170629.2:c.2273A>T
MANE Select
|
NP_001164100.1:p.Asp758Val
|
|
NM_020920.4:c.1436A>T
|
NP_065971.2:p.Asp479Val
|
|