ENST00000450892.7:c.5234A>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Gln1745Arg
|
|
ENST00000411560.1:n.142+432T>C
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2267A>G
(STRC)
|
ENSP00000415991.1:n.*2267A>G
|
|
ENST00000440125.5:c.*3026A>G
(STRC)
|
ENSP00000394866.1:n.*3026A>G
|
|
ENST00000448437.6:n.2354A>G
(STRC)
|
|
|
ENST00000450892.6:c.5234A>G
(STRC)
|
ENSP00000401513.2:p.Gln1745Arg
|
|
ENST00000471703.5:n.3188A>G
(STRC)
|
|
|
ENST00000485556.5:n.4089A>G
(STRC)
|
|
|
ENST00000541030.5:c.2915A>G
(STRC)
|
ENSP00000440413.1:p.Gln972Arg
|
|
NM_153700.2:c.5234A>G
(STRC)
MANE Select
|
NP_714544.1:p.Gln1745Arg
|
|
XM_011521277.1:c.5723A>G
(STRC)
|
XP_011519579.1:p.Gln1908Arg
|
|
XM_011521278.1:c.5339A>G
(STRC)
|
XP_011519580.1:p.Gln1780Arg
|
|
XM_011521279.1:c.5339A>G
(STRC)
|
XP_011519581.1:p.Gln1780Arg
|
|