ENST00000450892.7:c.5233C>T
(STRC)
MANE Select
|
ENSP00000401513.2:p.Gln1745Ter
|
|
ENST00000411560.1:n.142+433G>A
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2266C>T
(STRC)
|
ENSP00000415991.1:n.*2266C>T
|
|
ENST00000440125.5:c.*3025C>T
(STRC)
|
ENSP00000394866.1:n.*3025C>T
|
|
ENST00000448437.6:n.2353C>T
(STRC)
|
|
|
ENST00000450892.6:c.5233C>T
(STRC)
|
ENSP00000401513.2:p.Gln1745Ter
|
|
ENST00000471703.5:n.3187C>T
(STRC)
|
|
|
ENST00000485556.5:n.4088C>T
(STRC)
|
|
|
ENST00000541030.5:c.2914C>T
(STRC)
|
ENSP00000440413.1:p.Gln972Ter
|
|
NM_153700.2:c.5233C>T
(STRC)
MANE Select
|
NP_714544.1:p.Gln1745Ter
|
|
XM_011521277.1:c.5722C>T
(STRC)
|
XP_011519579.1:p.Gln1908Ter
|
|
XM_011521278.1:c.5338C>T
(STRC)
|
XP_011519580.1:p.Gln1780Ter
|
|
XM_011521279.1:c.5338C>T
(STRC)
|
XP_011519581.1:p.Gln1780Ter
|
|