ENST00000369538.4:c.1191A>C
|
ENSP00000358551.4:p.Glu397Asp
|
|
ENST00000520113.7:c.1203A>C
MANE Select
|
ENSP00000430075.3:p.Glu401Asp
|
|
ENST00000637080.1:c.986A>C
|
ENSP00000489753.1:n.986A>C
|
|
ENST00000639077.1:n.868A>C
|
|
|
ENST00000369538.3:c.1290A>C
|
ENSP00000358551.3:p.Glu430Asp
|
|
ENST00000520113.6:c.1302A>C
|
ENSP00000430075.2:p.Glu434Asp
|
|
NM_000036.2:c.1302A>C
|
NP_000027.2:p.Glu434Asp
|
|
NM_001172626.1:c.1290A>C
|
NP_001166097.1:p.Glu430Asp
|
|
NM_000036.3:c.1203A>C
MANE Select
|
NP_000027.3:p.Glu401Asp
|
|
NM_001172626.2:c.1191A>C
|
NP_001166097.2:p.Glu397Asp
|
|