|
ENST00000450892.7:c.4012C>T
(STRC)
MANE Select
|
ENSP00000401513.2:p.Arg1338Ter
|
|
|
ENST00000411560.1:n.143-19G>A
(CKMT1B)
|
|
|
|
ENST00000428650.5:c.*1215C>T
(STRC)
|
ENSP00000415991.1:n.*1215C>T
|
|
|
ENST00000440125.5:c.*1804C>T
(STRC)
|
ENSP00000394866.1:n.*1804C>T
|
|
|
ENST00000448437.6:n.1665+3098C>T
(STRC)
|
|
|
|
ENST00000450892.6:c.4012C>T
(STRC)
|
ENSP00000401513.2:p.Arg1338Ter
|
|
|
ENST00000455136.5:c.1043C>T
(STRC)
|
|
|
|
ENST00000471703.5:n.1966C>T
(STRC)
|
|
|
|
ENST00000485556.5:n.2867C>T
(STRC)
|
|
|
|
ENST00000541030.5:c.1693C>T
(STRC)
|
ENSP00000440413.1:p.Arg565Ter
|
|
|
NM_153700.2:c.4012C>T
(STRC)
MANE Select
|
NP_714544.1:p.Arg1338Ter
|
|
|
XM_011521277.1:c.4501C>T
(STRC)
|
XP_011519579.1:p.Arg1501Ter
|
|
|
XM_011521278.1:c.4117C>T
(STRC)
|
XP_011519580.1:p.Arg1373Ter
|
|
|
XM_011521279.1:c.4117C>T
(STRC)
|
XP_011519581.1:p.Arg1373Ter
|
|
