ENST00000369538.4:c.382G=
|
ENSP00000358551.4:p.Asp128=
|
|
ENST00000520113.7:c.394G=
MANE Select
|
ENSP00000430075.3:p.Asp132=
|
|
ENST00000637080.1:c.397G=
|
ENSP00000489753.1:p.Asp133=
|
|
ENST00000639077.1:n.59G=
|
|
|
ENST00000369538.3:c.481G=
|
ENSP00000358551.3:p.Asp161=
|
|
ENST00000485564.3:n.268G=
|
|
|
ENST00000520113.6:c.493G=
|
ENSP00000430075.2:p.Asp165=
|
|
NM_000036.2:c.493G=
|
NP_000027.2:p.Asp165=
|
|
NM_001172626.1:c.481G=
|
NP_001166097.1:p.Asp161=
|
|
NM_000036.3:c.394G=
MANE Select
|
NP_000027.3:p.Asp132=
|
|
NM_001172626.2:c.382G=
|
NP_001166097.2:p.Asp128=
|
|