ENST00000682617.1:c.2358C>A
|
ENSP00000507912.1:p.Arg786=
|
|
ENST00000683962.1:c.*1914C>A
|
ENSP00000506854.1:n.*1914C>A
|
|
ENST00000311895.8:c.2220C>A
MANE Select
|
ENSP00000310520.7:p.Arg740=
|
|
ENST00000311895.7:c.2220C>A
|
ENSP00000310520.7:p.Arg740=
|
|
ENST00000389138.7:n.1497C>A
|
|
|
ENST00000462862.1:c.533C>A
|
ENSP00000461322.1:n.533C>A
|
|
NM_005236.2:c.2220C>A , LRG_463t1:c.2220C>A
|
NP_005227.1:p.Arg740=
|
|
XM_011522424.1:c.2358C>A
|
XP_011520726.1:p.Arg786=
|
|
XM_011522425.1:c.1677C>A
|
XP_011520727.1:p.Arg559=
|
|
XM_011522426.1:c.1431C>A
|
XP_011520728.1:p.Arg477=
|
|
XM_011522427.1:c.870C>A
|
XP_011520729.1:p.Arg290=
|
|
XR_932805.1:n.2379C>A
|
|
|
XM_011522424.3:c.2358C>A
|
XP_011520726.1:p.Arg786=
|
|
XM_017023043.2:c.1431C>A
|
XP_016878532.1:p.Arg477=
|
|
NM_005236.3:c.2220C>A
MANE Select
|
NP_005227.1:p.Arg740=
|
|