ENST00000450892.7:c.4952A>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Asn1651Thr
|
|
ENST00000411560.1:n.142+1042T>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1985A>C
(STRC)
|
ENSP00000415991.1:n.*1985A>C
|
|
ENST00000440125.5:c.*2744A>C
(STRC)
|
ENSP00000394866.1:n.*2744A>C
|
|
ENST00000448437.6:n.2072A>C
(STRC)
|
|
|
ENST00000450892.6:c.4952A>C
(STRC)
|
ENSP00000401513.2:p.Asn1651Thr
|
|
ENST00000460952.1:n.531A>C
(STRC)
|
|
|
ENST00000471703.5:n.2906A>C
(STRC)
|
|
|
ENST00000485556.5:n.3807A>C
(STRC)
|
|
|
ENST00000541030.5:c.2633A>C
(STRC)
|
ENSP00000440413.1:p.Asn878Thr
|
|
NM_153700.2:c.4952A>C
(STRC)
MANE Select
|
NP_714544.1:p.Asn1651Thr
|
|
XM_011521277.1:c.5441A>C
(STRC)
|
XP_011519579.1:p.Asn1814Thr
|
|
XM_011521278.1:c.5057A>C
(STRC)
|
XP_011519580.1:p.Asn1686Thr
|
|
XM_011521279.1:c.5057A>C
(STRC)
|
XP_011519581.1:p.Asn1686Thr
|
|