ENST00000369538.4:c.522G>C
|
ENSP00000358551.4:p.Glu174Asp
|
|
ENST00000520113.7:c.534G>C
MANE Select
|
ENSP00000430075.3:p.Glu178Asp
|
|
ENST00000637080.1:c.537G>C
|
ENSP00000489753.1:p.Glu179Asp
|
|
ENST00000639077.1:n.199G>C
|
|
|
ENST00000369538.3:c.621G>C
|
ENSP00000358551.3:p.Glu207Asp
|
|
ENST00000485564.3:n.408G>C
|
|
|
ENST00000520113.6:c.633G>C
|
ENSP00000430075.2:p.Glu211Asp
|
|
NM_000036.2:c.633G>C
|
NP_000027.2:p.Glu211Asp
|
|
NM_001172626.1:c.621G>C
|
NP_001166097.1:p.Glu207Asp
|
|
NM_000036.3:c.534G>C
MANE Select
|
NP_000027.3:p.Glu178Asp
|
|
NM_001172626.2:c.522G>C
|
NP_001166097.2:p.Glu174Asp
|
|