ENST00000262367.10:c.5410C>G
MANE Select
|
ENSP00000262367.5:p.His1804Asp
|
|
ENST00000262367.9:c.5410C>G
|
ENSP00000262367.5:p.His1804Asp
|
|
ENST00000382070.7:c.5296C>G
|
ENSP00000371502.3:p.His1766Asp
|
|
NM_001079846.1:c.5296C>G
|
NP_001073315.1:p.His1766Asp
|
|
NM_004380.2:c.5410C>G
|
NP_004371.2:p.His1804Asp
|
|
XM_005255124.3:c.5365C>G
|
XP_005255181.1:p.His1789Asp
|
|
XM_005255125.3:c.4993C>G
|
XP_005255182.1:p.His1665Asp
|
|
XM_006720848.2:c.5149C>G
|
XP_006720911.1:p.His1717Asp
|
|
XM_011522380.1:c.5356C>G
|
XP_011520682.1:p.His1786Asp
|
|
XM_011522381.1:c.4657C>G
|
XP_011520683.1:p.His1553Asp
|
|
XM_005255124.4:c.5365C>G
|
XP_005255181.1:p.His1789Asp
|
|
XM_005255125.4:c.4993C>G
|
XP_005255182.1:p.His1665Asp
|
|
XM_006720848.3:c.5149C>G
|
XP_006720911.1:p.His1717Asp
|
|
XM_011522381.2:c.4657C>G
|
XP_011520683.1:p.His1553Asp
|
|
XM_017022944.1:c.5404C>G
|
XP_016878433.1:p.His1802Asp
|
|
NM_004380.3:c.5410C>G
MANE Select
|
NP_004371.2:p.His1804Asp
|
|