ENST00000450892.7:c.4626A>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Glu1542Asp
|
|
ENST00000411560.1:n.142+1938T>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1659A>C
(STRC)
|
ENSP00000415991.1:n.*1659A>C
|
|
ENST00000440125.5:c.*2418A>C
(STRC)
|
ENSP00000394866.1:n.*2418A>C
|
|
ENST00000448437.6:n.1746A>C
(STRC)
|
|
|
ENST00000450892.6:c.4626A>C
(STRC)
|
ENSP00000401513.2:p.Glu1542Asp
|
|
ENST00000460952.1:n.205A>C
(STRC)
|
|
|
ENST00000471703.5:n.2580A>C
(STRC)
|
|
|
ENST00000485556.5:n.3481A>C
(STRC)
|
|
|
ENST00000493750.1:n.422A>C
(STRC)
|
|
|
ENST00000541030.5:c.2307A>C
(STRC)
|
ENSP00000440413.1:p.Glu769Asp
|
|
NM_153700.2:c.4626A>C
(STRC)
MANE Select
|
NP_714544.1:p.Glu1542Asp
|
|
XM_011521277.1:c.5115A>C
(STRC)
|
XP_011519579.1:p.Glu1705Asp
|
|
XM_011521278.1:c.4731A>C
(STRC)
|
XP_011519580.1:p.Glu1577Asp
|
|
XM_011521279.1:c.4731A>C
(STRC)
|
XP_011519581.1:p.Glu1577Asp
|
|