ENST00000368485.8:c.1269G>T
MANE Select
|
ENSP00000357470.3:p.Val423=
|
|
ENST00000344086.8:c.*77G>T
|
ENSP00000340589.4:n.*77G>T
|
|
ENST00000368485.7:c.1269G>T
|
ENSP00000357470.3:p.Val423=
|
|
ENST00000502679.1:n.582G>T
|
|
|
ENST00000507256.1:n.467G>T
|
|
|
NM_000565.3:c.1269G>T
|
NP_000556.1:p.Val423=
|
|
NM_181359.2:c.*77G>T
|
NP_852004.1:n.*77G>T
|
|
XM_005245139.1:c.1033G>T
|
XP_005245196.1:p.Ala345Ser
|
|
XM_005245140.1:c.*110G>T
|
XP_005245197.1:n.*110G>T
|
|
XM_006711298.1:c.1317G>T
|
XP_006711361.1:p.Val439=
|
|
XM_006711299.2:c.*77G>T
|
XP_006711362.1:n.*77G>T
|
|
XM_005245139.2:c.1033G>T
|
XP_005245196.1:p.Ala345Ser
|
|
XM_005245140.3:c.*110G>T
|
XP_005245197.1:n.*110G>T
|
|
XM_006711298.2:c.1317G>T
|
XP_006711361.1:p.Val439=
|
|
XM_006711299.4:c.*77G>T
|
XP_006711362.1:n.*77G>T
|
|
XM_017001199.2:c.1416G>T
|
XP_016856688.1:p.Val472=
|
|
XM_017001200.2:c.1368G>T
|
XP_016856689.1:p.Val456=
|
|
XM_017001201.2:c.*110G>T
|
XP_016856690.1:n.*110G>T
|
|
NM_000565.4:c.1269G>T
MANE Select
|
NP_000556.1:p.Val423=
|
|
NM_181359.3:c.*77G>T
|
NP_852004.1:n.*77G>T
|
|
NM_001382769.1:c.1368G>T
|
NP_001369698.1:p.Val456=
|
|
NM_001382770.1:c.1362G>T
|
NP_001369699.1:p.Val454=
|
|
NM_001382771.1:c.1317G>T
|
NP_001369700.1:p.Val439=
|
|
NM_001382772.1:c.1263G>T
|
NP_001369701.1:p.Val421=
|
|
NM_001382773.1:c.*77G>T
|
NP_001369702.1:n.*77G>T
|
|
NM_001382774.1:c.909G>T
|
NP_001369703.1:p.Val303=
|
|