ENST00000369538.4:c.861C>T
|
ENSP00000358551.4:p.His287=
|
|
ENST00000520113.7:c.873C>T
MANE Select
|
ENSP00000430075.3:p.His291=
|
|
ENST00000637080.1:c.656C>T
|
ENSP00000489753.1:n.656C>T
|
|
ENST00000639077.1:n.538C>T
|
|
|
ENST00000369538.3:c.960C>T
|
ENSP00000358551.3:p.His320=
|
|
ENST00000520113.6:c.972C>T
|
ENSP00000430075.2:p.His324=
|
|
NM_000036.2:c.972C>T
|
NP_000027.2:p.His324=
|
|
NM_001172626.1:c.960C>T
|
NP_001166097.1:p.His320=
|
|
NM_000036.3:c.873C>T
MANE Select
|
NP_000027.3:p.His291=
|
|
NM_001172626.2:c.861C>T
|
NP_001166097.2:p.His287=
|
|