ENST00000267845.8:c.1781C>A
MANE Select
|
ENSP00000267845.3:p.Ala594Asp
|
|
ENST00000267845.7:c.1781C>A
|
ENSP00000267845.3:p.Ala594Asp
|
|
ENST00000543581.5:c.1682C>A
|
ENSP00000440252.1:p.Ala561Asp
|
|
ENST00000559816.1:n.1525C>A
|
|
|
NM_001306146.1:c.1682C>A
|
NP_001293075.1:p.Ala561Asp
|
|
NM_002112.3:c.1781C>A
|
NP_002103.2:p.Ala594Asp
|
|
XM_011521479.1:c.1544C>A
|
XP_011519781.1:p.Ala515Asp
|
|
XM_011521480.1:c.1349C>A
|
XP_011519782.1:p.Ala450Asp
|
|
XM_017022094.1:c.1886C>A
|
XP_016877583.1:p.Ala629Asp
|
|
XM_017022095.1:c.1787C>A
|
XP_016877584.1:p.Ala596Asp
|
|
XM_017022096.1:c.1658C>A
|
XP_016877585.1:p.Ala553Asp
|
|
XM_017022097.1:c.1649C>A
|
XP_016877586.1:p.Ala550Asp
|
|
XM_017022098.1:c.1454C>A
|
XP_016877587.1:p.Ala485Asp
|
|
NM_002112.4:c.1781C>A
MANE Select
|
NP_002103.2:p.Ala594Asp
|
|
NM_001306146.2:c.1682C>A
|
NP_001293075.1:p.Ala561Asp
|
|