|
NM_001754.5:c.812G>A
MANE Select
|
NP_001745.2:p.Arg271Lys
|
|
ENST00000675419.1:c.812G>A
MANE Select
|
ENSP00000501943.1:p.Arg271Lys
|
|
NM_001001890.2:c.731G>A
|
NP_001001890.1:p.Arg244Lys
|
|
NM_001001890.3:c.731G>A
|
NP_001001890.1:p.Arg244Lys
|
|
NM_001754.4:c.812G>A , LRG_482t1:c.812G>A
|
NP_001745.2:p.Arg271Lys
|
|
ENST00000300305.7:c.812G>A
|
ENSP00000300305.3:p.Arg271Lys
|
|
ENST00000344691.8:c.731G>A
|
ENSP00000340690.4:p.Arg244Lys
|
|
ENST00000399240.5:c.539G>A
|
ENSP00000382184.1:p.Arg180Lys
|
|
ENST00000437180.5:c.812G>A
|
ENSP00000409227.1:p.Arg271Lys
|
|
ENST00000482318.5:c.*402G>A
|
ENSP00000477067.1:n.*402G>A
|
|
XM_005261068.3:c.776G>A
|
XP_005261125.1:p.Arg259Lys
|
|
XM_005261069.3:c.620G>A
|
XP_005261126.1:p.Arg207Lys
|
|
XM_005261069.4:c.620G>A
|
XP_005261126.1:p.Arg207Lys
|
|
XM_011529766.1:c.812G>A
|
XP_011528068.1:p.Arg271Lys
|
|
XM_011529766.2:c.812G>A
|
XP_011528068.1:p.Arg271Lys
|
|
XM_011529767.1:c.773G>A
|
XP_011528069.1:p.Arg258Lys
|
|
XM_011529767.2:c.773G>A
|
XP_011528069.1:p.Arg258Lys
|
|
XM_011529768.1:c.581G>A
|
XP_011528070.1:p.Arg194Lys
|
|
XM_011529768.2:c.581G>A
|
XP_011528070.1:p.Arg194Lys
|
|
XM_017028487.1:c.659G>A
|
XP_016883976.1:p.Arg220Lys
|
|
XR_937576.1:n.991G>A
|
|
|
XR_937576.2:n.1038G>A
|
|
