ENST00000267845.8:c.1802A>T
MANE Select
|
ENSP00000267845.3:p.Glu601Val
|
|
ENST00000267845.7:c.1802A>T
|
ENSP00000267845.3:p.Glu601Val
|
|
ENST00000543581.5:c.1703A>T
|
ENSP00000440252.1:p.Glu568Val
|
|
ENST00000559816.1:n.1546A>T
|
|
|
NM_001306146.1:c.1703A>T
|
NP_001293075.1:p.Glu568Val
|
|
NM_002112.3:c.1802A>T
|
NP_002103.2:p.Glu601Val
|
|
XM_011521479.1:c.1565A>T
|
XP_011519781.1:p.Glu522Val
|
|
XM_011521480.1:c.1370A>T
|
XP_011519782.1:p.Glu457Val
|
|
XM_017022094.1:c.1907A>T
|
XP_016877583.1:p.Glu636Val
|
|
XM_017022095.1:c.1808A>T
|
XP_016877584.1:p.Glu603Val
|
|
XM_017022096.1:c.1679A>T
|
XP_016877585.1:p.Glu560Val
|
|
XM_017022097.1:c.1670A>T
|
XP_016877586.1:p.Glu557Val
|
|
XM_017022098.1:c.1475A>T
|
XP_016877587.1:p.Glu492Val
|
|
NM_002112.4:c.1802A>T
MANE Select
|
NP_002103.2:p.Glu601Val
|
|
NM_001306146.2:c.1703A>T
|
NP_001293075.1:p.Glu568Val
|
|