ENST00000450892.7:c.5268C>T
(STRC)
MANE Select
|
ENSP00000401513.2:p.Asp1756=
|
|
ENST00000411560.1:n.142+199G>A
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2301C>T
(STRC)
|
ENSP00000415991.1:n.*2301C>T
|
|
ENST00000440125.5:c.*3060C>T
(STRC)
|
ENSP00000394866.1:n.*3060C>T
|
|
ENST00000448437.6:n.2388C>T
(STRC)
|
|
|
ENST00000450892.6:c.5268C>T
(STRC)
|
ENSP00000401513.2:p.Asp1756=
|
|
ENST00000471703.5:n.3222C>T
(STRC)
|
|
|
ENST00000485556.5:n.4123C>T
(STRC)
|
|
|
ENST00000541030.5:c.2949C>T
(STRC)
|
ENSP00000440413.1:p.Asp983=
|
|
NM_153700.2:c.5268C>T
(STRC)
MANE Select
|
NP_714544.1:p.Asp1756=
|
|
XM_011521277.1:c.5757C>T
(STRC)
|
XP_011519579.1:p.Asp1919=
|
|
XM_011521278.1:c.5373C>T
(STRC)
|
XP_011519580.1:p.Asp1791=
|
|
XM_011521279.1:c.5373C>T
(STRC)
|
XP_011519581.1:p.Asp1791=
|
|