ENST00000450892.7:c.5286G>A
(STRC)
MANE Select
|
ENSP00000401513.2:p.Trp1762Ter
|
|
ENST00000411560.1:n.142+181C>T
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2319G>A
(STRC)
|
ENSP00000415991.1:n.*2319G>A
|
|
ENST00000440125.5:c.*3078G>A
(STRC)
|
ENSP00000394866.1:n.*3078G>A
|
|
ENST00000448437.6:n.2406G>A
(STRC)
|
|
|
ENST00000450892.6:c.5286G>A
(STRC)
|
ENSP00000401513.2:p.Trp1762Ter
|
|
ENST00000471703.5:n.3240G>A
(STRC)
|
|
|
ENST00000485556.5:n.4141G>A
(STRC)
|
|
|
ENST00000541030.5:c.2967G>A
(STRC)
|
ENSP00000440413.1:p.Trp989Ter
|
|
NM_153700.2:c.5286G>A
(STRC)
MANE Select
|
NP_714544.1:p.Trp1762Ter
|
|
XM_011521277.1:c.5775G>A
(STRC)
|
XP_011519579.1:p.Trp1925Ter
|
|
XM_011521278.1:c.5391G>A
(STRC)
|
XP_011519580.1:p.Trp1797Ter
|
|
XM_011521279.1:c.5391G>A
(STRC)
|
XP_011519581.1:p.Trp1797Ter
|
|