|
NM_001754.5:c.865G>C
MANE Select
|
NP_001745.2:p.Gly289Arg
|
|
ENST00000675419.1:c.865G>C
MANE Select
|
ENSP00000501943.1:p.Gly289Arg
|
|
NM_001001890.2:c.784G>C
|
NP_001001890.1:p.Gly262Arg
|
|
NM_001001890.3:c.784G>C
|
NP_001001890.1:p.Gly262Arg
|
|
NM_001754.4:c.865G>C , LRG_482t1:c.865G>C
|
NP_001745.2:p.Gly289Arg
|
|
ENST00000300305.7:c.865G>C
|
ENSP00000300305.3:p.Gly289Arg
|
|
ENST00000344691.8:c.784G>C
|
ENSP00000340690.4:p.Gly262Arg
|
|
ENST00000399240.5:c.592G>C
|
ENSP00000382184.1:p.Gly198Arg
|
|
ENST00000437180.5:c.865G>C
|
ENSP00000409227.1:p.Gly289Arg
|
|
ENST00000482318.5:c.*455G>C
|
ENSP00000477067.1:n.*455G>C
|
|
XM_005261068.3:c.829G>C
|
XP_005261125.1:p.Gly277Arg
|
|
XM_005261069.3:c.673G>C
|
XP_005261126.1:p.Gly225Arg
|
|
XM_005261069.4:c.673G>C
|
XP_005261126.1:p.Gly225Arg
|
|
XM_011529766.1:c.865G>C
|
XP_011528068.1:p.Gly289Arg
|
|
XM_011529766.2:c.865G>C
|
XP_011528068.1:p.Gly289Arg
|
|
XM_011529767.1:c.826G>C
|
XP_011528069.1:p.Gly276Arg
|
|
XM_011529767.2:c.826G>C
|
XP_011528069.1:p.Gly276Arg
|
|
XM_011529768.1:c.634G>C
|
XP_011528070.1:p.Gly212Arg
|
|
XM_011529768.2:c.634G>C
|
XP_011528070.1:p.Gly212Arg
|
|
XM_017028487.1:c.712G>C
|
XP_016883976.1:p.Gly238Arg
|
|
XR_937576.1:n.1044G>C
|
|
|
XR_937576.2:n.1091G>C
|
|
