ENST00000682617.1:c.2101G>T
|
ENSP00000507912.1:p.Asp701Tyr
|
|
ENST00000683962.1:c.*1657G>T
|
ENSP00000506854.1:n.*1657G>T
|
|
ENST00000311895.8:c.1963G>T
MANE Select
|
ENSP00000310520.7:p.Asp655Tyr
|
|
ENST00000311895.7:c.1963G>T
|
ENSP00000310520.7:p.Asp655Tyr
|
|
ENST00000389138.7:n.1240G>T
|
|
|
ENST00000462862.1:c.276G>T
|
ENSP00000461322.1:n.276G>T
|
|
NM_005236.2:c.1963G>T , LRG_463t1:c.1963G>T
|
NP_005227.1:p.Asp655Tyr
|
|
XM_011522424.1:c.2101G>T
|
XP_011520726.1:p.Asp701Tyr
|
|
XM_011522425.1:c.1420G>T
|
XP_011520727.1:p.Asp474Tyr
|
|
XM_011522426.1:c.1174G>T
|
XP_011520728.1:p.Asp392Tyr
|
|
XM_011522427.1:c.613G>T
|
XP_011520729.1:p.Asp205Tyr
|
|
XR_932805.1:n.2122G>T
|
|
|
XM_011522424.3:c.2101G>T
|
XP_011520726.1:p.Asp701Tyr
|
|
XM_017023043.2:c.1174G>T
|
XP_016878532.1:p.Asp392Tyr
|
|
NM_005236.3:c.1963G>T
MANE Select
|
NP_005227.1:p.Asp655Tyr
|
|