ENST00000369538.4:c.422G>A
|
ENSP00000358551.4:p.Cys141Tyr
|
|
ENST00000520113.7:c.434G>A
MANE Select
|
ENSP00000430075.3:p.Cys145Tyr
|
|
ENST00000637080.1:c.437G>A
|
ENSP00000489753.1:p.Cys146Tyr
|
|
ENST00000639077.1:n.99G>A
|
|
|
ENST00000369538.3:c.521G>A
|
ENSP00000358551.3:p.Cys174Tyr
|
|
ENST00000485564.3:n.308G>A
|
|
|
ENST00000520113.6:c.533G>A
|
ENSP00000430075.2:p.Cys178Tyr
|
|
NM_000036.2:c.533G>A
|
NP_000027.2:p.Cys178Tyr
|
|
NM_001172626.1:c.521G>A
|
NP_001166097.1:p.Cys174Tyr
|
|
NM_000036.3:c.434G>A
MANE Select
|
NP_000027.3:p.Cys145Tyr
|
|
NM_001172626.2:c.422G>A
|
NP_001166097.2:p.Cys141Tyr
|
|