ENST00000450892.7:c.5238A>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Gln1746His
|
|
ENST00000411560.1:n.142+428T>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2271A>C
(STRC)
|
ENSP00000415991.1:n.*2271A>C
|
|
ENST00000440125.5:c.*3030A>C
(STRC)
|
ENSP00000394866.1:n.*3030A>C
|
|
ENST00000448437.6:n.2358A>C
(STRC)
|
|
|
ENST00000450892.6:c.5238A>C
(STRC)
|
ENSP00000401513.2:p.Gln1746His
|
|
ENST00000471703.5:n.3192A>C
(STRC)
|
|
|
ENST00000485556.5:n.4093A>C
(STRC)
|
|
|
ENST00000541030.5:c.2919A>C
(STRC)
|
ENSP00000440413.1:p.Gln973His
|
|
NM_153700.2:c.5238A>C
(STRC)
MANE Select
|
NP_714544.1:p.Gln1746His
|
|
XM_011521277.1:c.5727A>C
(STRC)
|
XP_011519579.1:p.Gln1909His
|
|
XM_011521278.1:c.5343A>C
(STRC)
|
XP_011519580.1:p.Gln1781His
|
|
XM_011521279.1:c.5343A>C
(STRC)
|
XP_011519581.1:p.Gln1781His
|
|