ENST00000368485.8:c.1257A>T
MANE Select
|
ENSP00000357470.3:p.Arg419=
|
|
ENST00000344086.8:c.*65A>T
|
ENSP00000340589.4:n.*65A>T
|
|
ENST00000368485.7:c.1257A>T
|
ENSP00000357470.3:p.Arg419=
|
|
ENST00000502679.1:n.570A>T
|
|
|
ENST00000507256.1:n.455A>T
|
|
|
NM_000565.3:c.1257A>T
|
NP_000556.1:p.Arg419=
|
|
NM_181359.2:c.*65A>T
|
NP_852004.1:n.*65A>T
|
|
XM_005245139.1:c.1021A>T
|
XP_005245196.1:p.Thr341Ser
|
|
XM_005245140.1:c.*98A>T
|
XP_005245197.1:n.*98A>T
|
|
XM_006711298.1:c.1305A>T
|
XP_006711361.1:p.Arg435=
|
|
XM_006711299.2:c.*65A>T
|
XP_006711362.1:n.*65A>T
|
|
XM_005245139.2:c.1021A>T
|
XP_005245196.1:p.Thr341Ser
|
|
XM_005245140.3:c.*98A>T
|
XP_005245197.1:n.*98A>T
|
|
XM_006711298.2:c.1305A>T
|
XP_006711361.1:p.Arg435=
|
|
XM_006711299.4:c.*65A>T
|
XP_006711362.1:n.*65A>T
|
|
XM_017001199.2:c.1404A>T
|
XP_016856688.1:p.Arg468=
|
|
XM_017001200.2:c.1356A>T
|
XP_016856689.1:p.Arg452=
|
|
XM_017001201.2:c.*98A>T
|
XP_016856690.1:n.*98A>T
|
|
NM_000565.4:c.1257A>T
MANE Select
|
NP_000556.1:p.Arg419=
|
|
NM_181359.3:c.*65A>T
|
NP_852004.1:n.*65A>T
|
|
NM_001382769.1:c.1356A>T
|
NP_001369698.1:p.Arg452=
|
|
NM_001382770.1:c.1350A>T
|
NP_001369699.1:p.Arg450=
|
|
NM_001382771.1:c.1305A>T
|
NP_001369700.1:p.Arg435=
|
|
NM_001382772.1:c.1251A>T
|
NP_001369701.1:p.Arg417=
|
|
NM_001382773.1:c.*65A>T
|
NP_001369702.1:n.*65A>T
|
|
NM_001382774.1:c.897A>T
|
NP_001369703.1:p.Arg299=
|
|