ENST00000450892.7:c.4671G>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Leu1557=
|
|
ENST00000411560.1:n.142+1893C>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1704G>C
(STRC)
|
ENSP00000415991.1:n.*1704G>C
|
|
ENST00000440125.5:c.*2463G>C
(STRC)
|
ENSP00000394866.1:n.*2463G>C
|
|
ENST00000448437.6:n.1791G>C
(STRC)
|
|
|
ENST00000450892.6:c.4671G>C
(STRC)
|
ENSP00000401513.2:p.Leu1557=
|
|
ENST00000460952.1:n.250G>C
(STRC)
|
|
|
ENST00000471703.5:n.2625G>C
(STRC)
|
|
|
ENST00000485556.5:n.3526G>C
(STRC)
|
|
|
ENST00000493750.1:n.467G>C
(STRC)
|
|
|
ENST00000541030.5:c.2352G>C
(STRC)
|
ENSP00000440413.1:p.Leu784=
|
|
NM_153700.2:c.4671G>C
(STRC)
MANE Select
|
NP_714544.1:p.Leu1557=
|
|
XM_011521277.1:c.5160G>C
(STRC)
|
XP_011519579.1:p.Leu1720=
|
|
XM_011521278.1:c.4776G>C
(STRC)
|
XP_011519580.1:p.Leu1592=
|
|
XM_011521279.1:c.4776G>C
(STRC)
|
XP_011519581.1:p.Leu1592=
|
|