ENST00000394329.9:c.14830C>G
MANE Select
|
ENSP00000377862.4:p.His4944Asp
|
|
ENST00000674496.2:c.9601C>G
|
ENSP00000501473.2:p.His3201Asp
|
|
ENST00000335110.5:c.9547C>G
|
ENSP00000335169.5:p.His3183Asp
|
|
ENST00000394329.7:c.14824C>G
|
ENSP00000377862.3:p.His4942Asp
|
|
NM_001291285.1:c.14827C>G
|
NP_001278214.1:p.His4943Asp
|
|
NM_001291303.1:c.14830C>G
|
NP_001278232.1:p.His4944Asp
|
|
NM_024582.4:c.14824C>G
|
NP_078858.4:p.His4942Asp
|
|
XM_011532236.1:c.14830C>G
|
XP_011530538.1:p.His4944Asp
|
|
XM_011532237.1:c.9601C>G
|
XP_011530539.1:p.His3201Asp
|
|
XM_011532236.2:c.14830C>G
|
XP_011530538.1:p.His4944Asp
|
|
XM_011532237.2:c.9601C>G
|
XP_011530539.1:p.His3201Asp
|
|
NM_001291285.2:c.14827C>G
|
NP_001278214.1:p.His4943Asp
|
|
NM_001291303.3:c.14830C>G
MANE Select
|
NP_001278232.1:p.His4944Asp
|
|
NM_024582.5:c.14824C>G
|
NP_078858.4:p.His4942Asp
|
|
NM_001291285.3:c.14827C>G
|
NP_001278214.1:p.His4943Asp
|
|
NM_024582.6:c.14824C>G
|
NP_078858.4:p.His4942Asp
|
|