ENST00000430710.8:c.1522A>C
|
ENSP00000406288.3:p.Arg508=
|
|
ENST00000555935.2:c.35A>C
|
|
|
ENST00000555962.6:c.-110-6814A>C
|
ENSP00000495174.1:n.-110-6814A>C
|
|
ENST00000557364.6:c.2359A>C
|
ENSP00000451601.1:p.Arg787=
|
|
ENST00000643469.1:c.2359A>C
|
ENSP00000495070.1:p.Arg787=
|
|
ENST00000645140.1:c.2271A>C
|
|
|
ENST00000645206.1:n.873A>C
|
|
|
ENST00000645929.1:c.1522A>C
|
ENSP00000494402.1:p.Arg508=
|
|
ENST00000646340.1:c.2365A>C
|
ENSP00000496730.1:p.Arg789=
|
|
ENST00000646647.2:c.2359A>C
MANE Select
|
ENSP00000495240.1:p.Arg787=
|
|
ENST00000399982.6:c.2359A>C
|
ENSP00000382863.2:p.Arg787=
|
|
ENST00000430710.7:c.1522A>C
|
ENSP00000406288.3:p.Arg508=
|
|
ENST00000554384.1:n.227A>C
|
|
|
ENST00000555935.1:c.35A>C
|
|
|
ENST00000555962.5:n.151-6814A>C
|
|
|
ENST00000557364.5:c.2359A>C
|
ENSP00000451601.1:p.Arg787=
|
|
NM_001170629.1:c.2359A>C
|
NP_001164100.1:p.Arg787=
|
|
NM_020920.3:c.1522A>C
|
NP_065971.2:p.Arg508=
|
|
NM_001170629.2:c.2359A>C
MANE Select
|
NP_001164100.1:p.Arg787=
|
|
NM_020920.4:c.1522A>C
|
NP_065971.2:p.Arg508=
|
|