ENST00000368485.8:c.1386A>C
MANE Select
|
ENSP00000357470.3:p.Thr462=
|
|
ENST00000344086.8:c.*194A>C
|
ENSP00000340589.4:n.*194A>C
|
|
ENST00000368485.7:c.1386A>C
|
ENSP00000357470.3:p.Thr462=
|
|
NM_000565.3:c.1386A>C
|
NP_000556.1:p.Thr462=
|
|
NM_181359.2:c.*194A>C
|
NP_852004.1:n.*194A>C
|
|
XM_005245139.1:c.*67A>C
|
XP_005245196.1:n.*67A>C
|
|
XM_005245140.1:c.*227A>C
|
XP_005245197.1:n.*227A>C
|
|
XM_006711298.1:c.1434A>C
|
XP_006711361.1:p.Thr478=
|
|
XM_005245139.2:c.*67A>C
|
XP_005245196.1:n.*67A>C
|
|
XM_005245140.3:c.*227A>C
|
XP_005245197.1:n.*227A>C
|
|
XM_006711298.2:c.1434A>C
|
XP_006711361.1:p.Thr478=
|
|
XM_017001199.2:c.1533A>C
|
XP_016856688.1:p.Thr511=
|
|
XM_017001200.2:c.1485A>C
|
XP_016856689.1:p.Thr495=
|
|
XM_017001201.2:c.*227A>C
|
XP_016856690.1:n.*227A>C
|
|
NM_000565.4:c.1386A>C
MANE Select
|
NP_000556.1:p.Thr462=
|
|
NM_181359.3:c.*194A>C
|
NP_852004.1:n.*194A>C
|
|
NM_001382769.1:c.1485A>C
|
NP_001369698.1:p.Thr495=
|
|
NM_001382770.1:c.1479A>C
|
NP_001369699.1:p.Thr493=
|
|
NM_001382771.1:c.1434A>C
|
NP_001369700.1:p.Thr478=
|
|
NM_001382772.1:c.1380A>C
|
NP_001369701.1:p.Thr460=
|
|
NM_001382773.1:c.*194A>C
|
NP_001369702.1:n.*194A>C
|
|
NM_001382774.1:c.1026A>C
|
NP_001369703.1:p.Thr342=
|
|