ENST00000450892.7:c.4546T>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Leu1516Val
|
|
ENST00000411560.1:n.142+2018A>C
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1579T>G
(STRC)
|
ENSP00000415991.1:n.*1579T>G
|
|
ENST00000440125.5:c.*2338T>G
(STRC)
|
ENSP00000394866.1:n.*2338T>G
|
|
ENST00000448437.6:n.1666T>G
(STRC)
|
|
|
ENST00000450892.6:c.4546T>G
(STRC)
|
ENSP00000401513.2:p.Leu1516Val
|
|
ENST00000460952.1:n.125T>G
(STRC)
|
|
|
ENST00000471703.5:n.2500T>G
(STRC)
|
|
|
ENST00000485556.5:n.3401T>G
(STRC)
|
|
|
ENST00000493750.1:n.342T>G
(STRC)
|
|
|
ENST00000541030.5:c.2227T>G
(STRC)
|
ENSP00000440413.1:p.Leu743Val
|
|
NM_153700.2:c.4546T>G
(STRC)
MANE Select
|
NP_714544.1:p.Leu1516Val
|
|
XM_011521277.1:c.5035T>G
(STRC)
|
XP_011519579.1:p.Leu1679Val
|
|
XM_011521278.1:c.4651T>G
(STRC)
|
XP_011519580.1:p.Leu1551Val
|
|
XM_011521279.1:c.4651T>G
(STRC)
|
XP_011519581.1:p.Leu1551Val
|
|