ENST00000450892.7:c.5239G>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Gly1747Arg
|
|
ENST00000411560.1:n.142+427C>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2272G>C
(STRC)
|
ENSP00000415991.1:n.*2272G>C
|
|
ENST00000440125.5:c.*3031G>C
(STRC)
|
ENSP00000394866.1:n.*3031G>C
|
|
ENST00000448437.6:n.2359G>C
(STRC)
|
|
|
ENST00000450892.6:c.5239G>C
(STRC)
|
ENSP00000401513.2:p.Gly1747Arg
|
|
ENST00000471703.5:n.3193G>C
(STRC)
|
|
|
ENST00000485556.5:n.4094G>C
(STRC)
|
|
|
ENST00000541030.5:c.2920G>C
(STRC)
|
ENSP00000440413.1:p.Gly974Arg
|
|
NM_153700.2:c.5239G>C
(STRC)
MANE Select
|
NP_714544.1:p.Gly1747Arg
|
|
XM_011521277.1:c.5728G>C
(STRC)
|
XP_011519579.1:p.Gly1910Arg
|
|
XM_011521278.1:c.5344G>C
(STRC)
|
XP_011519580.1:p.Gly1782Arg
|
|
XM_011521279.1:c.5344G>C
(STRC)
|
XP_011519581.1:p.Gly1782Arg
|
|