ENST00000368485.8:c.1067-273G>T
MANE Select
|
ENSP00000357470.3:n.1067-273G>T
|
|
ENST00000344086.8:c.1066+4235G>T
|
ENSP00000340589.4:n.1066+4235G>T
|
|
ENST00000368485.7:c.1067-273G>T
|
ENSP00000357470.3:n.1067-273G>T
|
|
ENST00000502679.1:n.107G>T
|
|
|
ENST00000507256.1:n.265-273G>T
|
|
|
ENST00000515190.1:c.475-273G>T
|
|
|
NM_000565.3:c.1067-273G>T
|
NP_000556.1:n.1067-273G>T
|
|
NM_181359.2:c.1066+4235G>T
|
NP_852004.1:n.1066+4235G>T
|
|
XM_005245139.1:c.924+4235G>T
|
XP_005245196.1:n.924+4235G>T
|
|
XM_005245140.1:c.925-273G>T
|
XP_005245197.1:n.925-273G>T
|
|
XM_006711298.1:c.1115-273G>T
|
XP_006711361.1:n.1115-273G>T
|
|
XM_006711299.2:c.1114+4235G>T
|
XP_006711362.1:n.1114+4235G>T
|
|
XM_005245139.2:c.924+4235G>T
|
XP_005245196.1:n.924+4235G>T
|
|
XM_005245140.3:c.925-273G>T
|
XP_005245197.1:n.925-273G>T
|
|
XM_006711298.2:c.1115-273G>T
|
XP_006711361.1:n.1115-273G>T
|
|
XM_006711299.4:c.1114+4235G>T
|
XP_006711362.1:n.1114+4235G>T
|
|
XM_017001199.2:c.1213+44G>T
|
XP_016856688.1:n.1213+44G>T
|
|
XM_017001200.2:c.1165+44G>T
|
XP_016856689.1:n.1165+44G>T
|
|
XM_017001201.2:c.1023+44G>T
|
XP_016856690.1:n.1023+44G>T
|
|
NM_000565.4:c.1067-273G>T
MANE Select
|
NP_000556.1:n.1067-273G>T
|
|
NM_181359.3:c.1066+4235G>T
|
NP_852004.1:n.1066+4235G>T
|
|
NM_001382769.1:c.1165+44G>T
|
NP_001369698.1:n.1165+44G>T
|
|
NM_001382770.1:c.1160-273G>T
|
NP_001369699.1:n.1160-273G>T
|
|
NM_001382771.1:c.1115-273G>T
|
NP_001369700.1:n.1115-273G>T
|
|
NM_001382772.1:c.1061-273G>T
|
NP_001369701.1:n.1061-273G>T
|
|
NM_001382773.1:c.1114+4235G>T
|
NP_001369702.1:n.1114+4235G>T
|
|
NM_001382774.1:c.707-273G>T
|
NP_001369703.1:n.707-273G>T
|
|