ENST00000450892.7:c.4682A>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Asp1561Ala
|
|
ENST00000411560.1:n.142+1882T>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1715A>C
(STRC)
|
ENSP00000415991.1:n.*1715A>C
|
|
ENST00000440125.5:c.*2474A>C
(STRC)
|
ENSP00000394866.1:n.*2474A>C
|
|
ENST00000448437.6:n.1802A>C
(STRC)
|
|
|
ENST00000450892.6:c.4682A>C
(STRC)
|
ENSP00000401513.2:p.Asp1561Ala
|
|
ENST00000460952.1:n.261A>C
(STRC)
|
|
|
ENST00000471703.5:n.2636A>C
(STRC)
|
|
|
ENST00000485556.5:n.3537A>C
(STRC)
|
|
|
ENST00000493750.1:n.478A>C
(STRC)
|
|
|
ENST00000541030.5:c.2363A>C
(STRC)
|
ENSP00000440413.1:p.Asp788Ala
|
|
NM_153700.2:c.4682A>C
(STRC)
MANE Select
|
NP_714544.1:p.Asp1561Ala
|
|
XM_011521277.1:c.5171A>C
(STRC)
|
XP_011519579.1:p.Asp1724Ala
|
|
XM_011521278.1:c.4787A>C
(STRC)
|
XP_011519580.1:p.Asp1596Ala
|
|
XM_011521279.1:c.4787A>C
(STRC)
|
XP_011519581.1:p.Asp1596Ala
|
|