ENST00000369538.4:c.403G>T
|
ENSP00000358551.4:p.Gly135Cys
|
|
ENST00000520113.7:c.415G>T
MANE Select
|
ENSP00000430075.3:p.Gly139Cys
|
|
ENST00000637080.1:c.418G>T
|
ENSP00000489753.1:p.Gly140Cys
|
|
ENST00000639077.1:n.80G>T
|
|
|
ENST00000369538.3:c.502G>T
|
ENSP00000358551.3:p.Gly168Cys
|
|
ENST00000485564.3:n.289G>T
|
|
|
ENST00000520113.6:c.514G>T
|
ENSP00000430075.2:p.Gly172Cys
|
|
NM_000036.2:c.514G>T
|
NP_000027.2:p.Gly172Cys
|
|
NM_001172626.1:c.502G>T
|
NP_001166097.1:p.Gly168Cys
|
|
NM_000036.3:c.415G>T
MANE Select
|
NP_000027.3:p.Gly139Cys
|
|
NM_001172626.2:c.403G>T
|
NP_001166097.2:p.Gly135Cys
|
|