ENST00000450892.7:c.4047C>T
(STRC)
MANE Select
|
ENSP00000401513.2:p.Leu1349=
|
|
ENST00000411560.1:n.143-54G>A
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1250C>T
(STRC)
|
ENSP00000415991.1:n.*1250C>T
|
|
ENST00000440125.5:c.*1839C>T
(STRC)
|
ENSP00000394866.1:n.*1839C>T
|
|
ENST00000448437.6:n.1665+3133C>T
(STRC)
|
|
|
ENST00000450892.6:c.4047C>T
(STRC)
|
ENSP00000401513.2:p.Leu1349=
|
|
ENST00000455136.5:c.1078C>T
(STRC)
|
|
|
ENST00000471703.5:n.2001C>T
(STRC)
|
|
|
ENST00000485556.5:n.2902C>T
(STRC)
|
|
|
ENST00000541030.5:c.1728C>T
(STRC)
|
ENSP00000440413.1:p.Leu576=
|
|
NM_153700.2:c.4047C>T
(STRC)
MANE Select
|
NP_714544.1:p.Leu1349=
|
|
XM_011521277.1:c.4536C>T
(STRC)
|
XP_011519579.1:p.Leu1512=
|
|
XM_011521278.1:c.4152C>T
(STRC)
|
XP_011519580.1:p.Leu1384=
|
|
XM_011521279.1:c.4152C>T
(STRC)
|
XP_011519581.1:p.Leu1384=
|
|