ENST00000450892.7:c.5259C>A
(STRC)
MANE Select
|
ENSP00000401513.2:p.Gly1753=
|
|
ENST00000411560.1:n.142+208G>T
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2292C>A
(STRC)
|
ENSP00000415991.1:n.*2292C>A
|
|
ENST00000440125.5:c.*3051C>A
(STRC)
|
ENSP00000394866.1:n.*3051C>A
|
|
ENST00000448437.6:n.2379C>A
(STRC)
|
|
|
ENST00000450892.6:c.5259C>A
(STRC)
|
ENSP00000401513.2:p.Gly1753=
|
|
ENST00000471703.5:n.3213C>A
(STRC)
|
|
|
ENST00000485556.5:n.4114C>A
(STRC)
|
|
|
ENST00000541030.5:c.2940C>A
(STRC)
|
ENSP00000440413.1:p.Gly980=
|
|
NM_153700.2:c.5259C>A
(STRC)
MANE Select
|
NP_714544.1:p.Gly1753=
|
|
XM_011521277.1:c.5748C>A
(STRC)
|
XP_011519579.1:p.Gly1916=
|
|
XM_011521278.1:c.5364C>A
(STRC)
|
XP_011519580.1:p.Gly1788=
|
|
XM_011521279.1:c.5364C>A
(STRC)
|
XP_011519581.1:p.Gly1788=
|
|