ENST00000450892.7:c.4969T>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Phe1657Val
|
|
ENST00000411560.1:n.142+1025A>C
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2002T>G
(STRC)
|
ENSP00000415991.1:n.*2002T>G
|
|
ENST00000440125.5:c.*2761T>G
(STRC)
|
ENSP00000394866.1:n.*2761T>G
|
|
ENST00000448437.6:n.2089T>G
(STRC)
|
|
|
ENST00000450892.6:c.4969T>G
(STRC)
|
ENSP00000401513.2:p.Phe1657Val
|
|
ENST00000471703.5:n.2923T>G
(STRC)
|
|
|
ENST00000485556.5:n.3824T>G
(STRC)
|
|
|
ENST00000541030.5:c.2650T>G
(STRC)
|
ENSP00000440413.1:p.Phe884Val
|
|
NM_153700.2:c.4969T>G
(STRC)
MANE Select
|
NP_714544.1:p.Phe1657Val
|
|
XM_011521277.1:c.5458T>G
(STRC)
|
XP_011519579.1:p.Phe1820Val
|
|
XM_011521278.1:c.5074T>G
(STRC)
|
XP_011519580.1:p.Phe1692Val
|
|
XM_011521279.1:c.5074T>G
(STRC)
|
XP_011519581.1:p.Phe1692Val
|
|