ENST00000369538.4:c.1292A>C
|
ENSP00000358551.4:p.Glu431Ala
|
|
ENST00000520113.7:c.1304A>C
MANE Select
|
ENSP00000430075.3:p.Glu435Ala
|
|
ENST00000637080.1:c.1087A>C
|
ENSP00000489753.1:n.1087A>C
|
|
ENST00000639077.1:n.969A>C
|
|
|
ENST00000369538.3:c.1391A>C
|
ENSP00000358551.3:p.Glu464Ala
|
|
ENST00000520113.6:c.1403A>C
|
ENSP00000430075.2:p.Glu468Ala
|
|
NM_000036.2:c.1403A>C
|
NP_000027.2:p.Glu468Ala
|
|
NM_001172626.1:c.1391A>C
|
NP_001166097.1:p.Glu464Ala
|
|
NM_000036.3:c.1304A>C
MANE Select
|
NP_000027.3:p.Glu435Ala
|
|
NM_001172626.2:c.1292A>C
|
NP_001166097.2:p.Glu431Ala
|
|