ENST00000369538.4:c.1202C=
|
ENSP00000358551.4:p.Thr401=
|
|
ENST00000520113.7:c.1214C=
MANE Select
|
ENSP00000430075.3:p.Thr405=
|
|
ENST00000637080.1:c.997C=
|
ENSP00000489753.1:n.997C=
|
|
ENST00000639077.1:n.879C=
|
|
|
ENST00000369538.3:c.1301C=
|
ENSP00000358551.3:p.Thr434=
|
|
ENST00000520113.6:c.1313C=
|
ENSP00000430075.2:p.Thr438=
|
|
NM_000036.2:c.1313C=
|
NP_000027.2:p.Thr438=
|
|
NM_001172626.1:c.1301C=
|
NP_001166097.1:p.Thr434=
|
|
NM_000036.3:c.1214C=
MANE Select
|
NP_000027.3:p.Thr405=
|
|
NM_001172626.2:c.1202C=
|
NP_001166097.2:p.Thr401=
|
|