ENST00000450892.7:c.5279C>A
(STRC)
MANE Select
|
ENSP00000401513.2:p.Pro1760His
|
|
ENST00000411560.1:n.142+188G>T
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2312C>A
(STRC)
|
ENSP00000415991.1:n.*2312C>A
|
|
ENST00000440125.5:c.*3071C>A
(STRC)
|
ENSP00000394866.1:n.*3071C>A
|
|
ENST00000448437.6:n.2399C>A
(STRC)
|
|
|
ENST00000450892.6:c.5279C>A
(STRC)
|
ENSP00000401513.2:p.Pro1760His
|
|
ENST00000471703.5:n.3233C>A
(STRC)
|
|
|
ENST00000485556.5:n.4134C>A
(STRC)
|
|
|
ENST00000541030.5:c.2960C>A
(STRC)
|
ENSP00000440413.1:p.Pro987His
|
|
NM_153700.2:c.5279C>A
(STRC)
MANE Select
|
NP_714544.1:p.Pro1760His
|
|
XM_011521277.1:c.5768C>A
(STRC)
|
XP_011519579.1:p.Pro1923His
|
|
XM_011521278.1:c.5384C>A
(STRC)
|
XP_011519580.1:p.Pro1795His
|
|
XM_011521279.1:c.5384C>A
(STRC)
|
XP_011519581.1:p.Pro1795His
|
|