ENST00000369538.4:c.843G>C
|
ENSP00000358551.4:p.Glu281Asp
|
|
ENST00000520113.7:c.855G>C
MANE Select
|
ENSP00000430075.3:p.Glu285Asp
|
|
ENST00000637080.1:c.638G>C
|
ENSP00000489753.1:n.638G>C
|
|
ENST00000639077.1:n.520G>C
|
|
|
ENST00000369538.3:c.942G>C
|
ENSP00000358551.3:p.Glu314Asp
|
|
ENST00000520113.6:c.954G>C
|
ENSP00000430075.2:p.Glu318Asp
|
|
NM_000036.2:c.954G>C
|
NP_000027.2:p.Glu318Asp
|
|
NM_001172626.1:c.942G>C
|
NP_001166097.1:p.Glu314Asp
|
|
NM_000036.3:c.855G>C
MANE Select
|
NP_000027.3:p.Glu285Asp
|
|
NM_001172626.2:c.843G>C
|
NP_001166097.2:p.Glu281Asp
|
|