ENST00000430710.8:c.3555T>A
|
ENSP00000406288.3:p.Ile1185=
|
|
ENST00000555935.2:c.2068T>A
|
|
|
ENST00000555962.6:c.265-284T>A
|
ENSP00000495174.1:n.265-284T>A
|
|
ENST00000557364.6:c.4392T>A
|
ENSP00000451601.1:p.Ile1464=
|
|
ENST00000643469.1:c.4392T>A
|
ENSP00000495070.1:p.Ile1464=
|
|
ENST00000645206.1:n.2906T>A
|
|
|
ENST00000645929.1:c.3555T>A
|
ENSP00000494402.1:p.Ile1185=
|
|
ENST00000646340.1:c.4398T>A
|
ENSP00000496730.1:p.Ile1466=
|
|
ENST00000646558.1:n.1208T>A
|
|
|
ENST00000646647.2:c.4392T>A
MANE Select
|
ENSP00000495240.1:p.Ile1464=
|
|
ENST00000399982.6:c.4392T>A
|
ENSP00000382863.2:p.Ile1464=
|
|
ENST00000430710.7:c.3555T>A
|
ENSP00000406288.3:p.Ile1185=
|
|
ENST00000555935.1:c.2068T>A
|
|
|
ENST00000555962.5:n.525-284T>A
|
|
|
ENST00000557364.5:c.4392T>A
|
ENSP00000451601.1:p.Ile1464=
|
|
NM_001170629.1:c.4392T>A
|
NP_001164100.1:p.Ile1464=
|
|
NM_020920.3:c.3555T>A
|
NP_065971.2:p.Ile1185=
|
|
NM_001170629.2:c.4392T>A
MANE Select
|
NP_001164100.1:p.Ile1464=
|
|
NM_020920.4:c.3555T>A
|
NP_065971.2:p.Ile1185=
|
|