ENST00000450892.7:c.4824C>A
(STRC)
MANE Select
|
ENSP00000401513.2:p.His1608Gln
|
|
ENST00000411560.1:n.142+1359G>T
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1857C>A
(STRC)
|
ENSP00000415991.1:n.*1857C>A
|
|
ENST00000440125.5:c.*2616C>A
(STRC)
|
ENSP00000394866.1:n.*2616C>A
|
|
ENST00000448437.6:n.1944C>A
(STRC)
|
|
|
ENST00000450892.6:c.4824C>A
(STRC)
|
ENSP00000401513.2:p.His1608Gln
|
|
ENST00000460952.1:n.403C>A
(STRC)
|
|
|
ENST00000471703.5:n.2778C>A
(STRC)
|
|
|
ENST00000485556.5:n.3679C>A
(STRC)
|
|
|
ENST00000541030.5:c.2505C>A
(STRC)
|
ENSP00000440413.1:p.His835Gln
|
|
NM_153700.2:c.4824C>A
(STRC)
MANE Select
|
NP_714544.1:p.His1608Gln
|
|
XM_011521277.1:c.5313C>A
(STRC)
|
XP_011519579.1:p.His1771Gln
|
|
XM_011521278.1:c.4929C>A
(STRC)
|
XP_011519580.1:p.His1643Gln
|
|
XM_011521279.1:c.4929C>A
(STRC)
|
XP_011519581.1:p.His1643Gln
|
|