ENST00000450892.7:c.4608A>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Ile1536Met
|
|
ENST00000411560.1:n.142+1956T>C
(CKMT1B)
|
|
|
ENST00000428650.5:c.*1641A>G
(STRC)
|
ENSP00000415991.1:n.*1641A>G
|
|
ENST00000440125.5:c.*2400A>G
(STRC)
|
ENSP00000394866.1:n.*2400A>G
|
|
ENST00000448437.6:n.1728A>G
(STRC)
|
|
|
ENST00000450892.6:c.4608A>G
(STRC)
|
ENSP00000401513.2:p.Ile1536Met
|
|
ENST00000460952.1:n.187A>G
(STRC)
|
|
|
ENST00000471703.5:n.2562A>G
(STRC)
|
|
|
ENST00000485556.5:n.3463A>G
(STRC)
|
|
|
ENST00000493750.1:n.404A>G
(STRC)
|
|
|
ENST00000541030.5:c.2289A>G
(STRC)
|
ENSP00000440413.1:p.Ile763Met
|
|
NM_153700.2:c.4608A>G
(STRC)
MANE Select
|
NP_714544.1:p.Ile1536Met
|
|
XM_011521277.1:c.5097A>G
(STRC)
|
XP_011519579.1:p.Ile1699Met
|
|
XM_011521278.1:c.4713A>G
(STRC)
|
XP_011519580.1:p.Ile1571Met
|
|
XM_011521279.1:c.4713A>G
(STRC)
|
XP_011519581.1:p.Ile1571Met
|
|