ENST00000369538.4:c.405T>C
|
ENSP00000358551.4:p.Gly135=
|
|
ENST00000520113.7:c.417T>C
MANE Select
|
ENSP00000430075.3:p.Gly139=
|
|
ENST00000637080.1:c.420T>C
|
ENSP00000489753.1:p.Gly140=
|
|
ENST00000639077.1:n.82T>C
|
|
|
ENST00000369538.3:c.504T>C
|
ENSP00000358551.3:p.Gly168=
|
|
ENST00000485564.3:n.291T>C
|
|
|
ENST00000520113.6:c.516T>C
|
ENSP00000430075.2:p.Gly172=
|
|
NM_000036.2:c.516T>C
|
NP_000027.2:p.Gly172=
|
|
NM_001172626.1:c.504T>C
|
NP_001166097.1:p.Gly168=
|
|
NM_000036.3:c.417T>C
MANE Select
|
NP_000027.3:p.Gly139=
|
|
NM_001172626.2:c.405T>C
|
NP_001166097.2:p.Gly135=
|
|