ENST00000262367.10:c.7078C>A
MANE Select
|
ENSP00000262367.5:p.His2360Asn
|
|
ENST00000262367.9:c.7078C>A
|
ENSP00000262367.5:p.His2360Asn
|
|
ENST00000382070.7:c.6964C>A
|
ENSP00000371502.3:p.His2322Asn
|
|
NM_001079846.1:c.6964C>A
|
NP_001073315.1:p.His2322Asn
|
|
NM_004380.2:c.7078C>A
|
NP_004371.2:p.His2360Asn
|
|
XM_005255124.3:c.7033C>A
|
XP_005255181.1:p.His2345Asn
|
|
XM_005255125.3:c.6661C>A
|
XP_005255182.1:p.His2221Asn
|
|
XM_006720848.2:c.6817C>A
|
XP_006720911.1:p.His2273Asn
|
|
XM_011522380.1:c.7024C>A
|
XP_011520682.1:p.His2342Asn
|
|
XM_011522381.1:c.6325C>A
|
XP_011520683.1:p.His2109Asn
|
|
XM_005255124.4:c.7033C>A
|
XP_005255181.1:p.His2345Asn
|
|
XM_005255125.4:c.6661C>A
|
XP_005255182.1:p.His2221Asn
|
|
XM_006720848.3:c.6817C>A
|
XP_006720911.1:p.His2273Asn
|
|
XM_011522381.2:c.6325C>A
|
XP_011520683.1:p.His2109Asn
|
|
XM_017022944.1:c.7072C>A
|
XP_016878433.1:p.His2358Asn
|
|
NM_004380.3:c.7078C>A
MANE Select
|
NP_004371.2:p.His2360Asn
|
|