ENST00000450892.7:c.5225G=
(STRC)
MANE Select
|
ENSP00000401513.2:p.Ser1742=
|
|
ENST00000411560.1:n.142+441C=
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2258G=
(STRC)
|
ENSP00000415991.1:n.*2258G=
|
|
ENST00000440125.5:c.*3017G=
(STRC)
|
ENSP00000394866.1:n.*3017G=
|
|
ENST00000448437.6:n.2345G=
(STRC)
|
|
|
ENST00000450892.6:c.5225G=
(STRC)
|
ENSP00000401513.2:p.Ser1742=
|
|
ENST00000471703.5:n.3179G=
(STRC)
|
|
|
ENST00000485556.5:n.4080G=
(STRC)
|
|
|
ENST00000541030.5:c.2906G=
(STRC)
|
ENSP00000440413.1:p.Ser969=
|
|
NM_153700.2:c.5225G=
(STRC)
MANE Select
|
NP_714544.1:p.Ser1742=
|
|
XM_011521277.1:c.5714G=
(STRC)
|
XP_011519579.1:p.Ser1905=
|
|
XM_011521278.1:c.5330G=
(STRC)
|
XP_011519580.1:p.Ser1777=
|
|
XM_011521279.1:c.5330G=
(STRC)
|
XP_011519581.1:p.Ser1777=
|
|