ENST00000267845.8:c.1859A>T
MANE Select
|
ENSP00000267845.3:p.Glu620Val
|
|
ENST00000267845.7:c.1859A>T
|
ENSP00000267845.3:p.Glu620Val
|
|
ENST00000543581.5:c.1760A>T
|
ENSP00000440252.1:p.Glu587Val
|
|
ENST00000559816.1:n.1603A>T
|
|
|
NM_001306146.1:c.1760A>T
|
NP_001293075.1:p.Glu587Val
|
|
NM_002112.3:c.1859A>T
|
NP_002103.2:p.Glu620Val
|
|
XM_011521479.1:c.1622A>T
|
XP_011519781.1:p.Glu541Val
|
|
XM_011521480.1:c.1427A>T
|
XP_011519782.1:p.Glu476Val
|
|
XM_017022094.1:c.1964A>T
|
XP_016877583.1:p.Glu655Val
|
|
XM_017022095.1:c.1865A>T
|
XP_016877584.1:p.Glu622Val
|
|
XM_017022096.1:c.1736A>T
|
XP_016877585.1:p.Glu579Val
|
|
XM_017022097.1:c.1727A>T
|
XP_016877586.1:p.Glu576Val
|
|
XM_017022098.1:c.1532A>T
|
XP_016877587.1:p.Glu511Val
|
|
NM_002112.4:c.1859A>T
MANE Select
|
NP_002103.2:p.Glu620Val
|
|
NM_001306146.2:c.1760A>T
|
NP_001293075.1:p.Glu587Val
|
|