|
ENST00000675419.1:c.976G>T
MANE Select
|
ENSP00000501943.1:p.Asp326Tyr
|
|
|
ENST00000300305.7:c.976G>T
|
ENSP00000300305.3:p.Asp326Tyr
|
|
|
ENST00000344691.8:c.895G>T
|
ENSP00000340690.4:p.Asp299Tyr
|
|
|
ENST00000399240.5:c.703G>T
|
ENSP00000382184.1:p.Asp235Tyr
|
|
|
ENST00000437180.5:c.976G>T
|
ENSP00000409227.1:p.Asp326Tyr
|
|
|
ENST00000482318.5:c.*566G>T
|
ENSP00000477067.1:n.*566G>T
|
|
|
NM_001001890.2:c.895G>T
|
NP_001001890.1:p.Asp299Tyr
|
|
|
NM_001754.4:c.976G>T , LRG_482t1:c.976G>T
|
NP_001745.2:p.Asp326Tyr
|
|
|
XM_005261068.3:c.940G>T
|
XP_005261125.1:p.Asp314Tyr
|
|
|
XM_005261069.3:c.784G>T
|
XP_005261126.1:p.Asp262Tyr
|
|
|
XM_011529766.1:c.976G>T
|
XP_011528068.1:p.Asp326Tyr
|
|
|
XM_011529767.1:c.937G>T
|
XP_011528069.1:p.Asp313Tyr
|
|
|
XM_011529768.1:c.745G>T
|
XP_011528070.1:p.Asp249Tyr
|
|
|
XR_937576.1:n.4580G>T
|
|
|
|
XM_005261069.4:c.784G>T
|
XP_005261126.1:p.Asp262Tyr
|
|
|
XM_011529766.2:c.976G>T
|
XP_011528068.1:p.Asp326Tyr
|
|
|
XM_011529767.2:c.937G>T
|
XP_011528069.1:p.Asp313Tyr
|
|
|
XM_011529768.2:c.745G>T
|
XP_011528070.1:p.Asp249Tyr
|
|
|
XM_017028487.1:c.823G>T
|
XP_016883976.1:p.Asp275Tyr
|
|
|
XR_937576.2:n.4627G>T
|
|
|
|
NM_001001890.3:c.895G>T
|
NP_001001890.1:p.Asp299Tyr
|
|
|
NM_001754.5:c.976G>T
MANE Select
|
NP_001745.2:p.Asp326Tyr
|
|
