ENST00000369538.4:c.398G>A
|
ENSP00000358551.4:p.Cys133Tyr
|
|
ENST00000520113.7:c.410G>A
MANE Select
|
ENSP00000430075.3:p.Cys137Tyr
|
|
ENST00000637080.1:c.413G>A
|
ENSP00000489753.1:p.Cys138Tyr
|
|
ENST00000639077.1:n.75G>A
|
|
|
ENST00000369538.3:c.497G>A
|
ENSP00000358551.3:p.Cys166Tyr
|
|
ENST00000485564.3:n.284G>A
|
|
|
ENST00000520113.6:c.509G>A
|
ENSP00000430075.2:p.Cys170Tyr
|
|
NM_000036.2:c.509G>A
|
NP_000027.2:p.Cys170Tyr
|
|
NM_001172626.1:c.497G>A
|
NP_001166097.1:p.Cys166Tyr
|
|
NM_000036.3:c.410G>A
MANE Select
|
NP_000027.3:p.Cys137Tyr
|
|
NM_001172626.2:c.398G>A
|
NP_001166097.2:p.Cys133Tyr
|
|