ENST00000262367.10:c.6955C>A
MANE Select
|
ENSP00000262367.5:p.His2319Asn
|
|
ENST00000262367.9:c.6955C>A
|
ENSP00000262367.5:p.His2319Asn
|
|
ENST00000382070.7:c.6841C>A
|
ENSP00000371502.3:p.His2281Asn
|
|
NM_001079846.1:c.6841C>A
|
NP_001073315.1:p.His2281Asn
|
|
NM_004380.2:c.6955C>A
|
NP_004371.2:p.His2319Asn
|
|
XM_005255124.3:c.6910C>A
|
XP_005255181.1:p.His2304Asn
|
|
XM_005255125.3:c.6538C>A
|
XP_005255182.1:p.His2180Asn
|
|
XM_006720848.2:c.6694C>A
|
XP_006720911.1:p.His2232Asn
|
|
XM_011522380.1:c.6901C>A
|
XP_011520682.1:p.His2301Asn
|
|
XM_011522381.1:c.6202C>A
|
XP_011520683.1:p.His2068Asn
|
|
XM_005255124.4:c.6910C>A
|
XP_005255181.1:p.His2304Asn
|
|
XM_005255125.4:c.6538C>A
|
XP_005255182.1:p.His2180Asn
|
|
XM_006720848.3:c.6694C>A
|
XP_006720911.1:p.His2232Asn
|
|
XM_011522381.2:c.6202C>A
|
XP_011520683.1:p.His2068Asn
|
|
XM_017022944.1:c.6949C>A
|
XP_016878433.1:p.His2317Asn
|
|
NM_004380.3:c.6955C>A
MANE Select
|
NP_004371.2:p.His2319Asn
|
|