ENST00000695901.1:c.798+714T>C
|
ENSP00000512251.1:n.798+714T>C
|
|
ENST00000695911.1:c.837T>C
|
ENSP00000512262.1:n.837T>C
|
|
ENST00000695912.1:c.1056T>C
|
ENSP00000512263.1:p.Arg352=
|
|
ENST00000695913.1:c.*1812T>C
|
ENSP00000512264.1:n.*1812T>C
|
|
ENST00000695914.1:c.819T>C
|
ENSP00000512265.1:p.Arg273=
|
|
ENST00000695918.1:n.287T>C
|
|
|
ENST00000306721.8:c.1059T>C
MANE Select
|
ENSP00000306968.3:p.Arg353=
|
|
ENST00000306721.7:c.1059T>C
|
ENSP00000306968.3:p.Arg353=
|
|
ENST00000347703.7:c.822T>C
|
ENSP00000272789.4:p.Arg274=
|
|
ENST00000410019.3:c.696T>C
|
ENSP00000386833.3:p.Arg232=
|
|
ENST00000410101.7:c.927T>C
|
ENSP00000386656.3:p.Arg309=
|
|
ENST00000467411.5:n.1768+714T>C
|
|
|
ENST00000496441.5:n.1813T>C
|
|
|
NM_031942.4:c.1059T>C
|
NP_114148.3:p.Arg353=
|
|
NM_145810.2:c.822T>C
|
NP_665809.1:p.Arg274=
|
|
XM_011511957.1:c.978T>C
|
XP_011510259.1:p.Arg326=
|
|
XR_923034.1:n.1957T>C
|
|
|
NM_031942.5:c.1059T>C
MANE Select
|
NP_114148.3:p.Arg353=
|
|
NM_145810.3:c.822T>C
|
NP_665809.1:p.Arg274=
|
|