ENST00000369538.4:c.431A>T
|
ENSP00000358551.4:p.Glu144Val
|
|
ENST00000520113.7:c.443A>T
MANE Select
|
ENSP00000430075.3:p.Glu148Val
|
|
ENST00000637080.1:c.446A>T
|
ENSP00000489753.1:p.Glu149Val
|
|
ENST00000639077.1:n.108A>T
|
|
|
ENST00000369538.3:c.530A>T
|
ENSP00000358551.3:p.Glu177Val
|
|
ENST00000485564.3:n.317A>T
|
|
|
ENST00000520113.6:c.542A>T
|
ENSP00000430075.2:p.Glu181Val
|
|
NM_000036.2:c.542A>T
|
NP_000027.2:p.Glu181Val
|
|
NM_001172626.1:c.530A>T
|
NP_001166097.1:p.Glu177Val
|
|
NM_000036.3:c.443A>T
MANE Select
|
NP_000027.3:p.Glu148Val
|
|
NM_001172626.2:c.431A>T
|
NP_001166097.2:p.Glu144Val
|
|