ENST00000450892.7:c.4975G>C
(STRC)
MANE Select
|
ENSP00000401513.2:p.Glu1659Gln
|
|
ENST00000411560.1:n.142+1019C>G
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2008G>C
(STRC)
|
ENSP00000415991.1:n.*2008G>C
|
|
ENST00000440125.5:c.*2767G>C
(STRC)
|
ENSP00000394866.1:n.*2767G>C
|
|
ENST00000448437.6:n.2095G>C
(STRC)
|
|
|
ENST00000450892.6:c.4975G>C
(STRC)
|
ENSP00000401513.2:p.Glu1659Gln
|
|
ENST00000471703.5:n.2929G>C
(STRC)
|
|
|
ENST00000485556.5:n.3830G>C
(STRC)
|
|
|
ENST00000541030.5:c.2656G>C
(STRC)
|
ENSP00000440413.1:p.Glu886Gln
|
|
NM_153700.2:c.4975G>C
(STRC)
MANE Select
|
NP_714544.1:p.Glu1659Gln
|
|
XM_011521277.1:c.5464G>C
(STRC)
|
XP_011519579.1:p.Glu1822Gln
|
|
XM_011521278.1:c.5080G>C
(STRC)
|
XP_011519580.1:p.Glu1694Gln
|
|
XM_011521279.1:c.5080G>C
(STRC)
|
XP_011519581.1:p.Glu1694Gln
|
|