ENST00000450892.7:c.3218G>A
MANE Select
|
ENSP00000401513.2:p.Arg1073Gln
|
|
ENST00000428650.5:c.*250G>A
|
ENSP00000415991.1:n.*250G>A
|
|
ENST00000440125.5:c.*1215+263G>A
|
ENSP00000394866.1:n.*1215+263G>A
|
|
ENST00000448437.6:n.445G>A
|
|
|
ENST00000450892.6:c.3218G>A
|
ENSP00000401513.2:p.Arg1073Gln
|
|
ENST00000455136.5:c.529+263G>A
|
|
|
ENST00000470279.1:n.532G>A
|
|
|
ENST00000471703.5:n.357G>A
|
|
|
ENST00000483250.5:n.529G>A
|
|
|
ENST00000485556.5:n.588G>A
|
|
|
ENST00000541030.5:c.1104+263G>A
|
ENSP00000440413.1:n.1104+263G>A
|
|
NM_153700.2:c.3218G>A
MANE Select
|
NP_714544.1:p.Arg1073Gln
|
|
XM_011521277.1:c.3707G>A
|
XP_011519579.1:p.Arg1236Gln
|
|
XM_011521278.1:c.3320G>A
|
XP_011519580.1:p.Arg1107Gln
|
|
XM_011521279.1:c.3320G>A
|
XP_011519581.1:p.Arg1107Gln
|
|