ENST00000450892.7:c.4766T>A
(STRC)
MANE Select
|
ENSP00000401513.2:p.Val1589Asp
|
|
ENST00000411560.1:n.142+1417A>T
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1799T>A
(STRC)
|
ENSP00000415991.1:n.*1799T>A
|
|
ENST00000440125.5:c.*2558T>A
(STRC)
|
ENSP00000394866.1:n.*2558T>A
|
|
ENST00000448437.6:n.1886T>A
(STRC)
|
|
|
ENST00000450892.6:c.4766T>A
(STRC)
|
ENSP00000401513.2:p.Val1589Asp
|
|
ENST00000460952.1:n.345T>A
(STRC)
|
|
|
ENST00000471703.5:n.2720T>A
(STRC)
|
|
|
ENST00000485556.5:n.3621T>A
(STRC)
|
|
|
ENST00000541030.5:c.2447T>A
(STRC)
|
ENSP00000440413.1:p.Val816Asp
|
|
NM_153700.2:c.4766T>A
(STRC)
MANE Select
|
NP_714544.1:p.Val1589Asp
|
|
XM_011521277.1:c.5255T>A
(STRC)
|
XP_011519579.1:p.Val1752Asp
|
|
XM_011521278.1:c.4871T>A
(STRC)
|
XP_011519580.1:p.Val1624Asp
|
|
XM_011521279.1:c.4871T>A
(STRC)
|
XP_011519581.1:p.Val1624Asp
|
|