ENST00000262367.10:c.5494C>G
MANE Select
|
ENSP00000262367.5:p.His1832Asp
|
|
ENST00000262367.9:c.5494C>G
|
ENSP00000262367.5:p.His1832Asp
|
|
ENST00000382070.7:c.5380C>G
|
ENSP00000371502.3:p.His1794Asp
|
|
NM_001079846.1:c.5380C>G
|
NP_001073315.1:p.His1794Asp
|
|
NM_004380.2:c.5494C>G
|
NP_004371.2:p.His1832Asp
|
|
XM_005255124.3:c.5449C>G
|
XP_005255181.1:p.His1817Asp
|
|
XM_005255125.3:c.5077C>G
|
XP_005255182.1:p.His1693Asp
|
|
XM_006720848.2:c.5233C>G
|
XP_006720911.1:p.His1745Asp
|
|
XM_011522380.1:c.5440C>G
|
XP_011520682.1:p.His1814Asp
|
|
XM_011522381.1:c.4741C>G
|
XP_011520683.1:p.His1581Asp
|
|
XM_005255124.4:c.5449C>G
|
XP_005255181.1:p.His1817Asp
|
|
XM_005255125.4:c.5077C>G
|
XP_005255182.1:p.His1693Asp
|
|
XM_006720848.3:c.5233C>G
|
XP_006720911.1:p.His1745Asp
|
|
XM_011522381.2:c.4741C>G
|
XP_011520683.1:p.His1581Asp
|
|
XM_017022944.1:c.5488C>G
|
XP_016878433.1:p.His1830Asp
|
|
NM_004380.3:c.5494C>G
MANE Select
|
NP_004371.2:p.His1832Asp
|
|