ENST00000267845.8:c.1932A>C
MANE Select
|
ENSP00000267845.3:p.Glu644Asp
|
|
ENST00000267845.7:c.1932A>C
|
ENSP00000267845.3:p.Glu644Asp
|
|
ENST00000543581.5:c.1833A>C
|
ENSP00000440252.1:p.Glu611Asp
|
|
ENST00000559816.1:n.1676A>C
|
|
|
NM_001306146.1:c.1833A>C
|
NP_001293075.1:p.Glu611Asp
|
|
NM_002112.3:c.1932A>C
|
NP_002103.2:p.Glu644Asp
|
|
XM_011521479.1:c.1695A>C
|
XP_011519781.1:p.Glu565Asp
|
|
XM_011521480.1:c.1500A>C
|
XP_011519782.1:p.Glu500Asp
|
|
XM_017022094.1:c.2037A>C
|
XP_016877583.1:p.Glu679Asp
|
|
XM_017022095.1:c.1938A>C
|
XP_016877584.1:p.Glu646Asp
|
|
XM_017022096.1:c.1809A>C
|
XP_016877585.1:p.Glu603Asp
|
|
XM_017022097.1:c.1800A>C
|
XP_016877586.1:p.Glu600Asp
|
|
XM_017022098.1:c.1605A>C
|
XP_016877587.1:p.Glu535Asp
|
|
NM_002112.4:c.1932A>C
MANE Select
|
NP_002103.2:p.Glu644Asp
|
|
NM_001306146.2:c.1833A>C
|
NP_001293075.1:p.Glu611Asp
|
|