ENST00000369538.4:c.1299C>T
|
ENSP00000358551.4:p.Ser433=
|
|
ENST00000520113.7:c.1311C>T
MANE Select
|
ENSP00000430075.3:p.Ser437=
|
|
ENST00000637080.1:c.1094C>T
|
ENSP00000489753.1:n.1094C>T
|
|
ENST00000639077.1:n.976C>T
|
|
|
ENST00000369538.3:c.1398C>T
|
ENSP00000358551.3:p.Ser466=
|
|
ENST00000520113.6:c.1410C>T
|
ENSP00000430075.2:p.Ser470=
|
|
NM_000036.2:c.1410C>T
|
NP_000027.2:p.Ser470=
|
|
NM_001172626.1:c.1398C>T
|
NP_001166097.1:p.Ser466=
|
|
NM_000036.3:c.1311C>T
MANE Select
|
NP_000027.3:p.Ser437=
|
|
NM_001172626.2:c.1299C>T
|
NP_001166097.2:p.Ser433=
|
|