ENST00000369538.4:c.388G=
|
ENSP00000358551.4:p.Glu130=
|
|
ENST00000520113.7:c.400G=
MANE Select
|
ENSP00000430075.3:p.Glu134=
|
|
ENST00000637080.1:c.403G=
|
ENSP00000489753.1:p.Glu135=
|
|
ENST00000639077.1:n.65G=
|
|
|
ENST00000369538.3:c.487G=
|
ENSP00000358551.3:p.Glu163=
|
|
ENST00000485564.3:n.274G=
|
|
|
ENST00000520113.6:c.499G=
|
ENSP00000430075.2:p.Glu167=
|
|
NM_000036.2:c.499G=
|
NP_000027.2:p.Glu167=
|
|
NM_001172626.1:c.487G=
|
NP_001166097.1:p.Glu163=
|
|
NM_000036.3:c.400G=
MANE Select
|
NP_000027.3:p.Glu134=
|
|
NM_001172626.2:c.388G=
|
NP_001166097.2:p.Glu130=
|
|