|
ENST00000450892.7:c.3493C>T
MANE Select
|
ENSP00000401513.2:p.Gln1165Ter
|
|
|
ENST00000428650.5:c.*525C>T
|
ENSP00000415991.1:n.*525C>T
|
|
|
ENST00000440125.5:c.*1285C>T
|
ENSP00000394866.1:n.*1285C>T
|
|
|
ENST00000448437.6:n.1364C>T
|
|
|
|
ENST00000450892.6:c.3493C>T
|
ENSP00000401513.2:p.Gln1165Ter
|
|
|
ENST00000455136.5:c.530-983C>T
|
|
|
|
ENST00000471703.5:n.1276C>T
|
|
|
|
ENST00000485556.5:n.1507C>T
|
|
|
|
ENST00000541030.5:c.1174C>T
|
ENSP00000440413.1:p.Gln392Ter
|
|
|
NM_153700.2:c.3493C>T
MANE Select
|
NP_714544.1:p.Gln1165Ter
|
|
|
XM_011521277.1:c.3982C>T
|
XP_011519579.1:p.Gln1328Ter
|
|
|
XM_011521278.1:c.3598C>T
|
XP_011519580.1:p.Gln1200Ter
|
|
|
XM_011521279.1:c.3598C>T
|
XP_011519581.1:p.Gln1200Ter
|
|
