ENST00000682568.1:n.1778C>G
|
|
|
ENST00000682617.1:c.1838C>G
|
ENSP00000507912.1:p.Thr613Arg
|
|
ENST00000682826.1:c.*1014C>G
|
ENSP00000507274.1:n.*1014C>G
|
|
ENST00000682909.1:n.3740C>G
|
|
|
ENST00000683277.1:n.3345C>G
|
|
|
ENST00000683407.1:n.1708C>G
|
|
|
ENST00000683962.1:c.*1394C>G
|
ENSP00000506854.1:n.*1394C>G
|
|
ENST00000311895.8:c.1700C>G
MANE Select
|
ENSP00000310520.7:p.Thr567Arg
|
|
ENST00000311895.7:c.1700C>G
|
ENSP00000310520.7:p.Thr567Arg
|
|
ENST00000389138.7:n.977C>G
|
|
|
NM_005236.2:c.1700C>G , LRG_463t1:c.1700C>G
|
NP_005227.1:p.Thr567Arg
|
|
XM_011522424.1:c.1838C>G
|
XP_011520726.1:p.Thr613Arg
|
|
XM_011522425.1:c.1157C>G
|
XP_011520727.1:p.Thr386Arg
|
|
XM_011522426.1:c.911C>G
|
XP_011520728.1:p.Thr304Arg
|
|
XM_011522427.1:c.350C>G
|
XP_011520729.1:p.Thr117Arg
|
|
XR_932805.1:n.1859C>G
|
|
|
XM_011522424.3:c.1838C>G
|
XP_011520726.1:p.Thr613Arg
|
|
XM_017023043.2:c.911C>G
|
XP_016878532.1:p.Thr304Arg
|
|
NM_005236.3:c.1700C>G
MANE Select
|
NP_005227.1:p.Thr567Arg
|
|