ENST00000450892.7:c.5301T>G
(STRC)
MANE Select
|
ENSP00000401513.2:p.Thr1767=
|
|
ENST00000411560.1:n.142+166A>C
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2334T>G
(STRC)
|
ENSP00000415991.1:n.*2334T>G
|
|
ENST00000440125.5:c.*3093T>G
(STRC)
|
ENSP00000394866.1:n.*3093T>G
|
|
ENST00000448437.6:n.2421T>G
(STRC)
|
|
|
ENST00000450892.6:c.5301T>G
(STRC)
|
ENSP00000401513.2:p.Thr1767=
|
|
ENST00000471703.5:n.3255T>G
(STRC)
|
|
|
ENST00000485556.5:n.4156T>G
(STRC)
|
|
|
ENST00000541030.5:c.2982T>G
(STRC)
|
ENSP00000440413.1:p.Thr994=
|
|
NM_153700.2:c.5301T>G
(STRC)
MANE Select
|
NP_714544.1:p.Thr1767=
|
|
XM_011521277.1:c.5790T>G
(STRC)
|
XP_011519579.1:p.Thr1930=
|
|
XM_011521278.1:c.5406T>G
(STRC)
|
XP_011519580.1:p.Thr1802=
|
|
XM_011521279.1:c.5406T>G
(STRC)
|
XP_011519581.1:p.Thr1802=
|
|