ENST00000682568.1:n.1836C=
|
|
|
ENST00000682617.1:c.1896C=
|
ENSP00000507912.1:p.Thr632=
|
|
ENST00000682826.1:c.*1072C=
|
ENSP00000507274.1:n.*1072C=
|
|
ENST00000682909.1:n.3798C=
|
|
|
ENST00000683277.1:n.3403C=
|
|
|
ENST00000683407.1:n.1766C=
|
|
|
ENST00000683962.1:c.*1452C=
|
ENSP00000506854.1:n.*1452C=
|
|
ENST00000311895.8:c.1758C=
MANE Select
|
ENSP00000310520.7:p.Thr586=
|
|
ENST00000311895.7:c.1758C=
|
ENSP00000310520.7:p.Thr586=
|
|
ENST00000389138.7:n.1035C=
|
|
|
NM_005236.2:c.1758C= , LRG_463t1:c.1758C=
|
NP_005227.1:p.Thr586=
|
|
XM_011522424.1:c.1896C=
|
XP_011520726.1:p.Thr632=
|
|
XM_011522425.1:c.1215C=
|
XP_011520727.1:p.Thr405=
|
|
XM_011522426.1:c.969C=
|
XP_011520728.1:p.Thr323=
|
|
XM_011522427.1:c.408C=
|
XP_011520729.1:p.Thr136=
|
|
XR_932805.1:n.1917C=
|
|
|
XM_011522424.3:c.1896C=
|
XP_011520726.1:p.Thr632=
|
|
XM_017023043.2:c.969C=
|
XP_016878532.1:p.Thr323=
|
|
NM_005236.3:c.1758C=
MANE Select
|
NP_005227.1:p.Thr586=
|
|