ENST00000267845.8:c.1679C>A
MANE Select
|
ENSP00000267845.3:p.Ala560Asp
|
|
ENST00000267845.7:c.1679C>A
|
ENSP00000267845.3:p.Ala560Asp
|
|
ENST00000543581.5:c.1580C>A
|
ENSP00000440252.1:p.Ala527Asp
|
|
ENST00000559816.1:n.1423C>A
|
|
|
NM_001306146.1:c.1580C>A
|
NP_001293075.1:p.Ala527Asp
|
|
NM_002112.3:c.1679C>A
|
NP_002103.2:p.Ala560Asp
|
|
XM_011521479.1:c.1442C>A
|
XP_011519781.1:p.Ala481Asp
|
|
XM_011521480.1:c.1247C>A
|
XP_011519782.1:p.Ala416Asp
|
|
XM_017022094.1:c.1784C>A
|
XP_016877583.1:p.Ala595Asp
|
|
XM_017022095.1:c.1685C>A
|
XP_016877584.1:p.Ala562Asp
|
|
XM_017022096.1:c.1556C>A
|
XP_016877585.1:p.Ala519Asp
|
|
XM_017022097.1:c.1547C>A
|
XP_016877586.1:p.Ala516Asp
|
|
XM_017022098.1:c.1352C>A
|
XP_016877587.1:p.Ala451Asp
|
|
NM_002112.4:c.1679C>A
MANE Select
|
NP_002103.2:p.Ala560Asp
|
|
NM_001306146.2:c.1580C>A
|
NP_001293075.1:p.Ala527Asp
|
|