ENST00000267845.8:c.1802A>G
MANE Select
|
ENSP00000267845.3:p.Glu601Gly
|
|
ENST00000267845.7:c.1802A>G
|
ENSP00000267845.3:p.Glu601Gly
|
|
ENST00000543581.5:c.1703A>G
|
ENSP00000440252.1:p.Glu568Gly
|
|
ENST00000559816.1:n.1546A>G
|
|
|
NM_001306146.1:c.1703A>G
|
NP_001293075.1:p.Glu568Gly
|
|
NM_002112.3:c.1802A>G
|
NP_002103.2:p.Glu601Gly
|
|
XM_011521479.1:c.1565A>G
|
XP_011519781.1:p.Glu522Gly
|
|
XM_011521480.1:c.1370A>G
|
XP_011519782.1:p.Glu457Gly
|
|
XM_017022094.1:c.1907A>G
|
XP_016877583.1:p.Glu636Gly
|
|
XM_017022095.1:c.1808A>G
|
XP_016877584.1:p.Glu603Gly
|
|
XM_017022096.1:c.1679A>G
|
XP_016877585.1:p.Glu560Gly
|
|
XM_017022097.1:c.1670A>G
|
XP_016877586.1:p.Glu557Gly
|
|
XM_017022098.1:c.1475A>G
|
XP_016877587.1:p.Glu492Gly
|
|
NM_002112.4:c.1802A>G
MANE Select
|
NP_002103.2:p.Glu601Gly
|
|
NM_001306146.2:c.1703A>G
|
NP_001293075.1:p.Glu568Gly
|
|