ENST00000450892.7:c.4193C=
(STRC)
MANE Select
|
ENSP00000401513.2:p.Thr1398=
|
|
ENST00000411560.1:n.143-398G=
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1396C=
(STRC)
|
ENSP00000415991.1:n.*1396C=
|
|
ENST00000440125.5:c.*1985C=
(STRC)
|
ENSP00000394866.1:n.*1985C=
|
|
ENST00000448437.6:n.1666-2835C=
(STRC)
|
|
|
ENST00000450892.6:c.4193C=
(STRC)
|
ENSP00000401513.2:p.Thr1398=
|
|
ENST00000471703.5:n.2147C=
(STRC)
|
|
|
ENST00000485556.5:n.3048C=
(STRC)
|
|
|
ENST00000541030.5:c.1874C=
(STRC)
|
ENSP00000440413.1:p.Thr625=
|
|
NM_153700.2:c.4193C=
(STRC)
MANE Select
|
NP_714544.1:p.Thr1398=
|
|
XM_011521277.1:c.4682C=
(STRC)
|
XP_011519579.1:p.Thr1561=
|
|
XM_011521278.1:c.4298C=
(STRC)
|
XP_011519580.1:p.Thr1433=
|
|
XM_011521279.1:c.4298C=
(STRC)
|
XP_011519581.1:p.Thr1433=
|
|