NM_031291.4:c.206G>A
MANE Select
|
NP_112581.1:p.Cys69Tyr
|
ENST00000281154.6:c.206G>A
MANE Select
|
ENSP00000281154.4:p.Cys69Tyr
|
NM_001318467.1:c.206G>A
|
NP_001305396.1:p.Cys69Tyr
|
NM_001318467.2:c.206G>A
|
NP_001305396.1:p.Cys69Tyr
|
NM_031291.2:c.206G>A
|
NP_112581.1:p.Cys69Tyr
|
NM_031291.3:c.206G>A
|
NP_112581.1:p.Cys69Tyr
|
ENST00000281154.5:c.206G>A
|
ENSP00000281154.4:p.Cys69Tyr
|
XM_011532297.1:c.206G>A
|
XP_011530599.1:p.Cys69Tyr
|
XM_011532298.1:c.206G>A
|
XP_011530600.1:p.Cys69Tyr
|
XM_011532298.2:c.206G>A
|
XP_011530600.1:p.Cys69Tyr
|