ENST00000450892.7:c.4965G>A
(STRC)
MANE Select
|
ENSP00000401513.2:p.Glu1655=
|
|
ENST00000411560.1:n.142+1029C>T
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1998G>A
(STRC)
|
ENSP00000415991.1:n.*1998G>A
|
|
ENST00000440125.5:c.*2757G>A
(STRC)
|
ENSP00000394866.1:n.*2757G>A
|
|
ENST00000448437.6:n.2085G>A
(STRC)
|
|
|
ENST00000450892.6:c.4965G>A
(STRC)
|
ENSP00000401513.2:p.Glu1655=
|
|
ENST00000471703.5:n.2919G>A
(STRC)
|
|
|
ENST00000485556.5:n.3820G>A
(STRC)
|
|
|
ENST00000541030.5:c.2646G>A
(STRC)
|
ENSP00000440413.1:p.Glu882=
|
|
NM_153700.2:c.4965G>A
(STRC)
MANE Select
|
NP_714544.1:p.Glu1655=
|
|
XM_011521277.1:c.5454G>A
(STRC)
|
XP_011519579.1:p.Glu1818=
|
|
XM_011521278.1:c.5070G>A
(STRC)
|
XP_011519580.1:p.Glu1690=
|
|
XM_011521279.1:c.5070G>A
(STRC)
|
XP_011519581.1:p.Glu1690=
|
|