ENST00000682617.1:c.2186G>C
|
ENSP00000507912.1:p.Ser729Thr
|
|
ENST00000683962.1:c.*1742G>C
|
ENSP00000506854.1:n.*1742G>C
|
|
ENST00000311895.8:c.2048G>C
MANE Select
|
ENSP00000310520.7:p.Ser683Thr
|
|
ENST00000311895.7:c.2048G>C
|
ENSP00000310520.7:p.Ser683Thr
|
|
ENST00000389138.7:n.1325G>C
|
|
|
ENST00000462862.1:c.361G>C
|
ENSP00000461322.1:n.361G>C
|
|
NM_005236.2:c.2048G>C , LRG_463t1:c.2048G>C
|
NP_005227.1:p.Ser683Thr
|
|
XM_011522424.1:c.2186G>C
|
XP_011520726.1:p.Ser729Thr
|
|
XM_011522425.1:c.1505G>C
|
XP_011520727.1:p.Ser502Thr
|
|
XM_011522426.1:c.1259G>C
|
XP_011520728.1:p.Ser420Thr
|
|
XM_011522427.1:c.698G>C
|
XP_011520729.1:p.Ser233Thr
|
|
XR_932805.1:n.2207G>C
|
|
|
XM_011522424.3:c.2186G>C
|
XP_011520726.1:p.Ser729Thr
|
|
XM_017023043.2:c.1259G>C
|
XP_016878532.1:p.Ser420Thr
|
|
NM_005236.3:c.2048G>C
MANE Select
|
NP_005227.1:p.Ser683Thr
|
|