ENST00000284885.8:c.2599C>G
MANE Select
|
ENSP00000284885.3:p.His867Asp
|
|
ENST00000284885.7:c.2599C>G
|
ENSP00000284885.3:p.His867Asp
|
|
NM_002772.2:c.2599C>G
|
NP_002763.2:p.His867Asp
|
|
XM_011529654.1:c.2734C>G
|
XP_011527956.1:p.His912Asp
|
|
XM_011529655.1:c.2734C>G
|
XP_011527957.1:p.His912Asp
|
|
XM_011529656.1:c.2734C>G
|
XP_011527958.1:p.His912Asp
|
|
XM_011529657.1:c.2689C>G
|
XP_011527959.1:p.His897Asp
|
|
XM_011529658.1:c.2653C>G
|
XP_011527960.1:p.His885Asp
|
|
XM_011529659.1:c.2644C>G
|
XP_011527961.1:p.His882Asp
|
|
XM_011529654.2:c.2734C>G
|
XP_011527956.1:p.His912Asp
|
|
XM_011529656.2:c.2734C>G
|
XP_011527958.1:p.His912Asp
|
|
XM_011529657.2:c.2689C>G
|
XP_011527959.1:p.His897Asp
|
|
XM_011529658.2:c.2653C>G
|
XP_011527960.1:p.His885Asp
|
|
NM_002772.3:c.2599C>G
MANE Select
|
NP_002763.3:p.His867Asp
|
|