|
NM_001754.5:c.730G>A
MANE Select
|
NP_001745.2:p.Ala244Thr
|
|
ENST00000675419.1:c.730G>A
MANE Select
|
ENSP00000501943.1:p.Ala244Thr
|
|
NM_001001890.2:c.649G>A
|
NP_001001890.1:p.Ala217Thr
|
|
NM_001001890.3:c.649G>A
|
NP_001001890.1:p.Ala217Thr
|
|
NM_001122607.1:c.649G>A
|
NP_001116079.1:p.Ala217Thr
|
|
NM_001122607.2:c.649G>A
|
NP_001116079.1:p.Ala217Thr
|
|
NM_001754.4:c.730G>A , LRG_482t1:c.730G>A
|
NP_001745.2:p.Ala244Thr
|
|
ENST00000300305.7:c.730G>A
|
ENSP00000300305.3:p.Ala244Thr
|
|
ENST00000344691.8:c.649G>A
|
ENSP00000340690.4:p.Ala217Thr
|
|
ENST00000358356.9:c.649G>A
|
ENSP00000351123.5:p.Ala217Thr
|
|
ENST00000399237.6:c.694G>A
|
ENSP00000382182.2:p.Ala232Thr
|
|
ENST00000399240.5:c.532+24989G>A
|
ENSP00000382184.1:n.532+24989G>A
|
|
ENST00000437180.5:c.730G>A
|
ENSP00000409227.1:p.Ala244Thr
|
|
ENST00000469087.1:n.266G>A
|
|
|
ENST00000482318.5:c.*320G>A
|
ENSP00000477067.1:n.*320G>A
|
|
XM_005261068.3:c.694G>A
|
XP_005261125.1:p.Ala232Thr
|
|
XM_005261069.3:c.613+24989G>A
|
XP_005261126.1:n.613+24989G>A
|
|
XM_005261069.4:c.613+24989G>A
|
XP_005261126.1:n.613+24989G>A
|
|
XM_011529766.1:c.730G>A
|
XP_011528068.1:p.Ala244Thr
|
|
XM_011529766.2:c.730G>A
|
XP_011528068.1:p.Ala244Thr
|
|
XM_011529767.1:c.691G>A
|
XP_011528069.1:p.Ala231Thr
|
|
XM_011529767.2:c.691G>A
|
XP_011528069.1:p.Ala231Thr
|
|
XM_011529768.1:c.574+24989G>A
|
XP_011528070.1:n.574+24989G>A
|
|
XM_011529768.2:c.574+24989G>A
|
XP_011528070.1:n.574+24989G>A
|
|
XM_011529770.1:c.730G>A
|
XP_011528072.1:p.Ala244Thr
|
|
XM_011529770.2:c.730G>A
|
XP_011528072.1:p.Ala244Thr
|
|
XM_017028487.1:c.577G>A
|
XP_016883976.1:p.Ala193Thr
|
|
XR_937576.1:n.909G>A
|
|
|
XR_937576.2:n.956G>A
|
|
