ENST00000450892.7:c.4552G>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Gly1518Arg
|
|
ENST00000411560.1:n.142+2012C>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1585G>C
(STRC)
|
ENSP00000415991.1:n.*1585G>C
|
|
ENST00000440125.5:c.*2344G>C
(STRC)
|
ENSP00000394866.1:n.*2344G>C
|
|
ENST00000448437.6:n.1672G>C
(STRC)
|
|
|
ENST00000450892.6:c.4552G>C
(STRC)
|
ENSP00000401513.2:p.Gly1518Arg
|
|
ENST00000460952.1:n.131G>C
(STRC)
|
|
|
ENST00000471703.5:n.2506G>C
(STRC)
|
|
|
ENST00000485556.5:n.3407G>C
(STRC)
|
|
|
ENST00000493750.1:n.348G>C
(STRC)
|
|
|
ENST00000541030.5:c.2233G>C
(STRC)
|
ENSP00000440413.1:p.Gly745Arg
|
|
NM_153700.2:c.4552G>C
(STRC)
MANE Select
|
NP_714544.1:p.Gly1518Arg
|
|
XM_011521277.1:c.5041G>C
(STRC)
|
XP_011519579.1:p.Gly1681Arg
|
|
XM_011521278.1:c.4657G>C
(STRC)
|
XP_011519580.1:p.Gly1553Arg
|
|
XM_011521279.1:c.4657G>C
(STRC)
|
XP_011519581.1:p.Gly1553Arg
|
|