ENST00000450892.7:c.5284T=
(STRC)
MANE Select
|
ENSP00000401513.2:p.Trp1762=
|
|
ENST00000411560.1:n.142+183A=
(CKMT1B)
|
|
|
ENST00000428650.5:c.*2317T=
(STRC)
|
ENSP00000415991.1:n.*2317T=
|
|
ENST00000440125.5:c.*3076T=
(STRC)
|
ENSP00000394866.1:n.*3076T=
|
|
ENST00000448437.6:n.2404T=
(STRC)
|
|
|
ENST00000450892.6:c.5284T=
(STRC)
|
ENSP00000401513.2:p.Trp1762=
|
|
ENST00000471703.5:n.3238T=
(STRC)
|
|
|
ENST00000485556.5:n.4139T=
(STRC)
|
|
|
ENST00000541030.5:c.2965T=
(STRC)
|
ENSP00000440413.1:p.Trp989=
|
|
NM_153700.2:c.5284T=
(STRC)
MANE Select
|
NP_714544.1:p.Trp1762=
|
|
XM_011521277.1:c.5773T=
(STRC)
|
XP_011519579.1:p.Trp1925=
|
|
XM_011521278.1:c.5389T=
(STRC)
|
XP_011519580.1:p.Trp1797=
|
|
XM_011521279.1:c.5389T=
(STRC)
|
XP_011519581.1:p.Trp1797=
|
|