ENST00000369458.8:c.790T>A
MANE Select
|
ENSP00000358470.3:p.Ser264Thr
|
|
ENST00000328189.7:c.442T>A
|
ENSP00000328168.3:p.Ser148Thr
|
|
ENST00000359008.8:c.799T>A
|
ENSP00000351899.4:p.Ser267Thr
|
|
ENST00000369458.7:c.790T>A
|
ENSP00000358470.3:p.Ser264Thr
|
|
ENST00000539893.5:c.505T>A
|
ENSP00000444724.1:p.Ser169Thr
|
|
NM_001253849.1:c.505T>A
|
NP_001240778.1:p.Ser169Thr
|
|
NM_001253850.1:c.442T>A
|
NP_001240779.1:p.Ser148Thr
|
|
NM_024626.3:c.790T>A
|
NP_078902.2:p.Ser264Thr
|
|
NR_045603.1:n.985T>A
|
|
|
NR_045604.1:n.689T>A
|
|
|
XM_011542143.1:c.841T>A
|
XP_011540445.1:p.Ser281Thr
|
|
XM_011542144.1:c.844T>A
|
XP_011540446.1:p.Ser282Thr
|
|
XM_011542145.1:c.805T>A
|
XP_011540447.1:p.Ser269Thr
|
|
XM_011542143.2:c.940T>A
|
XP_011540445.2:p.Ser314Thr
|
|
XM_017002335.2:c.805T>A
|
XP_016857824.1:p.Ser269Thr
|
|
NM_024626.4:c.790T>A
MANE Select
|
NP_078902.2:p.Ser264Thr
|
|
NR_045603.2:n.952T>A
|
|
|
NR_045604.2:n.656T>A
|
|
|
NM_001253849.2:c.505T>A
|
NP_001240778.1:p.Ser169Thr
|
|
NM_001253850.2:c.442T>A
|
NP_001240779.1:p.Ser148Thr
|
|