ENST00000262367.10:c.6985C>G
MANE Select
|
ENSP00000262367.5:p.His2329Asp
|
|
ENST00000262367.9:c.6985C>G
|
ENSP00000262367.5:p.His2329Asp
|
|
ENST00000382070.7:c.6871C>G
|
ENSP00000371502.3:p.His2291Asp
|
|
NM_001079846.1:c.6871C>G
|
NP_001073315.1:p.His2291Asp
|
|
NM_004380.2:c.6985C>G
|
NP_004371.2:p.His2329Asp
|
|
XM_005255124.3:c.6940C>G
|
XP_005255181.1:p.His2314Asp
|
|
XM_005255125.3:c.6568C>G
|
XP_005255182.1:p.His2190Asp
|
|
XM_006720848.2:c.6724C>G
|
XP_006720911.1:p.His2242Asp
|
|
XM_011522380.1:c.6931C>G
|
XP_011520682.1:p.His2311Asp
|
|
XM_011522381.1:c.6232C>G
|
XP_011520683.1:p.His2078Asp
|
|
XM_005255124.4:c.6940C>G
|
XP_005255181.1:p.His2314Asp
|
|
XM_005255125.4:c.6568C>G
|
XP_005255182.1:p.His2190Asp
|
|
XM_006720848.3:c.6724C>G
|
XP_006720911.1:p.His2242Asp
|
|
XM_011522381.2:c.6232C>G
|
XP_011520683.1:p.His2078Asp
|
|
XM_017022944.1:c.6979C>G
|
XP_016878433.1:p.His2327Asp
|
|
NM_004380.3:c.6985C>G
MANE Select
|
NP_004371.2:p.His2329Asp
|
|