ENST00000430710.8:c.3552T>C
|
ENSP00000406288.3:p.Asp1184=
|
|
ENST00000555935.2:c.2065T>C
|
|
|
ENST00000555962.6:c.265-287T>C
|
ENSP00000495174.1:n.265-287T>C
|
|
ENST00000557364.6:c.4389T>C
|
ENSP00000451601.1:p.Asp1463=
|
|
ENST00000643469.1:c.4389T>C
|
ENSP00000495070.1:p.Asp1463=
|
|
ENST00000645206.1:n.2903T>C
|
|
|
ENST00000645929.1:c.3552T>C
|
ENSP00000494402.1:p.Asp1184=
|
|
ENST00000646340.1:c.4395T>C
|
ENSP00000496730.1:p.Asp1465=
|
|
ENST00000646558.1:n.1205T>C
|
|
|
ENST00000646647.2:c.4389T>C
MANE Select
|
ENSP00000495240.1:p.Asp1463=
|
|
ENST00000399982.6:c.4389T>C
|
ENSP00000382863.2:p.Asp1463=
|
|
ENST00000430710.7:c.3552T>C
|
ENSP00000406288.3:p.Asp1184=
|
|
ENST00000555935.1:c.2065T>C
|
|
|
ENST00000555962.5:n.525-287T>C
|
|
|
ENST00000557364.5:c.4389T>C
|
ENSP00000451601.1:p.Asp1463=
|
|
NM_001170629.1:c.4389T>C
|
NP_001164100.1:p.Asp1463=
|
|
NM_020920.3:c.3552T>C
|
NP_065971.2:p.Asp1184=
|
|
NM_001170629.2:c.4389T>C
MANE Select
|
NP_001164100.1:p.Asp1463=
|
|
NM_020920.4:c.3552T>C
|
NP_065971.2:p.Asp1184=
|
|