ENST00000450892.7:c.4803G>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Leu1601=
|
|
ENST00000411560.1:n.142+1380C>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1836G>C
(STRC)
|
ENSP00000415991.1:n.*1836G>C
|
|
ENST00000440125.5:c.*2595G>C
(STRC)
|
ENSP00000394866.1:n.*2595G>C
|
|
ENST00000448437.6:n.1923G>C
(STRC)
|
|
|
ENST00000450892.6:c.4803G>C
(STRC)
|
ENSP00000401513.2:p.Leu1601=
|
|
ENST00000460952.1:n.382G>C
(STRC)
|
|
|
ENST00000471703.5:n.2757G>C
(STRC)
|
|
|
ENST00000485556.5:n.3658G>C
(STRC)
|
|
|
ENST00000541030.5:c.2484G>C
(STRC)
|
ENSP00000440413.1:p.Leu828=
|
|
NM_153700.2:c.4803G>C
(STRC)
MANE Select
|
NP_714544.1:p.Leu1601=
|
|
XM_011521277.1:c.5292G>C
(STRC)
|
XP_011519579.1:p.Leu1764=
|
|
XM_011521278.1:c.4908G>C
(STRC)
|
XP_011519580.1:p.Leu1636=
|
|
XM_011521279.1:c.4908G>C
(STRC)
|
XP_011519581.1:p.Leu1636=
|
|