ENST00000450892.7:c.5317C>A
(STRC)
MANE Select
|
ENSP00000401513.2:p.His1773Asn
|
|
ENST00000411560.1:n.142+150G>T
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2350C>A
(STRC)
|
ENSP00000415991.1:n.*2350C>A
|
|
ENST00000440125.5:c.*3109C>A
(STRC)
|
ENSP00000394866.1:n.*3109C>A
|
|
ENST00000448437.6:n.2437C>A
(STRC)
|
|
|
ENST00000450892.6:c.5317C>A
(STRC)
|
ENSP00000401513.2:p.His1773Asn
|
|
ENST00000471703.5:n.3271C>A
(STRC)
|
|
|
ENST00000485556.5:n.4172C>A
(STRC)
|
|
|
ENST00000541030.5:c.2998C>A
(STRC)
|
ENSP00000440413.1:p.His1000Asn
|
|
NM_153700.2:c.5317C>A
(STRC)
MANE Select
|
NP_714544.1:p.His1773Asn
|
|
XM_011521277.1:c.5806C>A
(STRC)
|
XP_011519579.1:p.His1936Asn
|
|
XM_011521278.1:c.5422C>A
(STRC)
|
XP_011519580.1:p.His1808Asn
|
|
XM_011521279.1:c.5422C>A
(STRC)
|
XP_011519581.1:p.His1808Asn
|
|