ENST00000450892.7:c.5306G>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Ser1769Thr
|
|
ENST00000411560.1:n.142+161C>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2339G>C
(STRC)
|
ENSP00000415991.1:n.*2339G>C
|
|
ENST00000440125.5:c.*3098G>C
(STRC)
|
ENSP00000394866.1:n.*3098G>C
|
|
ENST00000448437.6:n.2426G>C
(STRC)
|
|
|
ENST00000450892.6:c.5306G>C
(STRC)
|
ENSP00000401513.2:p.Ser1769Thr
|
|
ENST00000471703.5:n.3260G>C
(STRC)
|
|
|
ENST00000485556.5:n.4161G>C
(STRC)
|
|
|
ENST00000541030.5:c.2987G>C
(STRC)
|
ENSP00000440413.1:p.Ser996Thr
|
|
NM_153700.2:c.5306G>C
(STRC)
MANE Select
|
NP_714544.1:p.Ser1769Thr
|
|
XM_011521277.1:c.5795G>C
(STRC)
|
XP_011519579.1:p.Ser1932Thr
|
|
XM_011521278.1:c.5411G>C
(STRC)
|
XP_011519580.1:p.Ser1804Thr
|
|
XM_011521279.1:c.5411G>C
(STRC)
|
XP_011519581.1:p.Ser1804Thr
|
|