ENST00000450892.7:c.4675C>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Gln1559Glu
|
|
ENST00000411560.1:n.142+1889G>C
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1708C>G
(STRC)
|
ENSP00000415991.1:n.*1708C>G
|
|
ENST00000440125.5:c.*2467C>G
(STRC)
|
ENSP00000394866.1:n.*2467C>G
|
|
ENST00000448437.6:n.1795C>G
(STRC)
|
|
|
ENST00000450892.6:c.4675C>G
(STRC)
|
ENSP00000401513.2:p.Gln1559Glu
|
|
ENST00000460952.1:n.254C>G
(STRC)
|
|
|
ENST00000471703.5:n.2629C>G
(STRC)
|
|
|
ENST00000485556.5:n.3530C>G
(STRC)
|
|
|
ENST00000493750.1:n.471C>G
(STRC)
|
|
|
ENST00000541030.5:c.2356C>G
(STRC)
|
ENSP00000440413.1:p.Gln786Glu
|
|
NM_153700.2:c.4675C>G
(STRC)
MANE Select
|
NP_714544.1:p.Gln1559Glu
|
|
XM_011521277.1:c.5164C>G
(STRC)
|
XP_011519579.1:p.Gln1722Glu
|
|
XM_011521278.1:c.4780C>G
(STRC)
|
XP_011519580.1:p.Gln1594Glu
|
|
XM_011521279.1:c.4780C>G
(STRC)
|
XP_011519581.1:p.Gln1594Glu
|
|