ENST00000430710.8:c.1459G>C
|
ENSP00000406288.3:p.Asp487His
|
|
ENST00000555962.6:c.-110-6877G>C
|
ENSP00000495174.1:n.-110-6877G>C
|
|
ENST00000557364.6:c.2296G>C
|
ENSP00000451601.1:p.Asp766His
|
|
ENST00000643469.1:c.2296G>C
|
ENSP00000495070.1:p.Asp766His
|
|
ENST00000645140.1:c.2208G>C
|
|
|
ENST00000645206.1:n.810G>C
|
|
|
ENST00000645929.1:c.1459G>C
|
ENSP00000494402.1:p.Asp487His
|
|
ENST00000646340.1:c.2302G>C
|
ENSP00000496730.1:p.Asp768His
|
|
ENST00000646647.2:c.2296G>C
MANE Select
|
ENSP00000495240.1:p.Asp766His
|
|
ENST00000399982.6:c.2296G>C
|
ENSP00000382863.2:p.Asp766His
|
|
ENST00000430710.7:c.1459G>C
|
ENSP00000406288.3:p.Asp487His
|
|
ENST00000554384.1:n.164G>C
|
|
|
ENST00000555962.5:n.151-6877G>C
|
|
|
ENST00000557364.5:c.2296G>C
|
ENSP00000451601.1:p.Asp766His
|
|
NM_001170629.1:c.2296G>C
|
NP_001164100.1:p.Asp766His
|
|
NM_020920.3:c.1459G>C
|
NP_065971.2:p.Asp487His
|
|
NM_001170629.2:c.2296G>C
MANE Select
|
NP_001164100.1:p.Asp766His
|
|
NM_020920.4:c.1459G>C
|
NP_065971.2:p.Asp487His
|
|