|
NM_001754.5:c.1197C>A
MANE Select
|
NP_001745.2:p.Ser399Arg
|
|
ENST00000675419.1:c.1197C>A
MANE Select
|
ENSP00000501943.1:p.Ser399Arg
|
|
NM_001001890.2:c.1116C>A
|
NP_001001890.1:p.Ser372Arg
|
|
NM_001001890.3:c.1116C>A
|
NP_001001890.1:p.Ser372Arg
|
|
NM_001754.4:c.1197C>A , LRG_482t1:c.1197C>A
|
NP_001745.2:p.Ser399Arg
|
|
ENST00000300305.7:c.1197C>A
|
ENSP00000300305.3:p.Ser399Arg
|
|
ENST00000344691.8:c.1116C>A
|
ENSP00000340690.4:p.Ser372Arg
|
|
ENST00000399240.5:c.924C>A
|
ENSP00000382184.1:p.Ser308Arg
|
|
ENST00000437180.5:c.1197C>A
|
ENSP00000409227.1:p.Ser399Arg
|
|
ENST00000482318.5:c.*787C>A
|
ENSP00000477067.1:n.*787C>A
|
|
XM_005261068.3:c.1161C>A
|
XP_005261125.1:p.Ser387Arg
|
|
XM_005261069.3:c.1005C>A
|
XP_005261126.1:p.Ser335Arg
|
|
XM_005261069.4:c.1005C>A
|
XP_005261126.1:p.Ser335Arg
|
|
XM_011529766.1:c.1197C>A
|
XP_011528068.1:p.Ser399Arg
|
|
XM_011529766.2:c.1197C>A
|
XP_011528068.1:p.Ser399Arg
|
|
XM_011529767.1:c.1158C>A
|
XP_011528069.1:p.Ser386Arg
|
|
XM_011529767.2:c.1158C>A
|
XP_011528069.1:p.Ser386Arg
|
|
XM_011529768.1:c.966C>A
|
XP_011528070.1:p.Ser322Arg
|
|
XM_011529768.2:c.966C>A
|
XP_011528070.1:p.Ser322Arg
|
|
XM_017028487.1:c.1044C>A
|
XP_016883976.1:p.Ser348Arg
|
