ENST00000262367.10:c.5569C>G
MANE Select
|
ENSP00000262367.5:p.His1857Asp
|
|
ENST00000262367.9:c.5569C>G
|
ENSP00000262367.5:p.His1857Asp
|
|
ENST00000382070.7:c.5455C>G
|
ENSP00000371502.3:p.His1819Asp
|
|
NM_001079846.1:c.5455C>G
|
NP_001073315.1:p.His1819Asp
|
|
NM_004380.2:c.5569C>G
|
NP_004371.2:p.His1857Asp
|
|
XM_005255124.3:c.5524C>G
|
XP_005255181.1:p.His1842Asp
|
|
XM_005255125.3:c.5152C>G
|
XP_005255182.1:p.His1718Asp
|
|
XM_006720848.2:c.5308C>G
|
XP_006720911.1:p.His1770Asp
|
|
XM_011522380.1:c.5515C>G
|
XP_011520682.1:p.His1839Asp
|
|
XM_011522381.1:c.4816C>G
|
XP_011520683.1:p.His1606Asp
|
|
XM_005255124.4:c.5524C>G
|
XP_005255181.1:p.His1842Asp
|
|
XM_005255125.4:c.5152C>G
|
XP_005255182.1:p.His1718Asp
|
|
XM_006720848.3:c.5308C>G
|
XP_006720911.1:p.His1770Asp
|
|
XM_011522381.2:c.4816C>G
|
XP_011520683.1:p.His1606Asp
|
|
XM_017022944.1:c.5563C>G
|
XP_016878433.1:p.His1855Asp
|
|
NM_004380.3:c.5569C>G
MANE Select
|
NP_004371.2:p.His1857Asp
|
|