ENST00000682617.1:c.2174G>T
|
ENSP00000507912.1:p.Gly725Val
|
|
ENST00000683962.1:c.*1730G>T
|
ENSP00000506854.1:n.*1730G>T
|
|
ENST00000311895.8:c.2036G>T
MANE Select
|
ENSP00000310520.7:p.Gly679Val
|
|
ENST00000311895.7:c.2036G>T
|
ENSP00000310520.7:p.Gly679Val
|
|
ENST00000389138.7:n.1313G>T
|
|
|
ENST00000462862.1:c.349G>T
|
ENSP00000461322.1:n.349G>T
|
|
NM_005236.2:c.2036G>T , LRG_463t1:c.2036G>T
|
NP_005227.1:p.Gly679Val
|
|
XM_011522424.1:c.2174G>T
|
XP_011520726.1:p.Gly725Val
|
|
XM_011522425.1:c.1493G>T
|
XP_011520727.1:p.Gly498Val
|
|
XM_011522426.1:c.1247G>T
|
XP_011520728.1:p.Gly416Val
|
|
XM_011522427.1:c.686G>T
|
XP_011520729.1:p.Gly229Val
|
|
XR_932805.1:n.2195G>T
|
|
|
XM_011522424.3:c.2174G>T
|
XP_011520726.1:p.Gly725Val
|
|
XM_017023043.2:c.1247G>T
|
XP_016878532.1:p.Gly416Val
|
|
NM_005236.3:c.2036G>T
MANE Select
|
NP_005227.1:p.Gly679Val
|
|