ENST00000262367.10:c.4273A>C
MANE Select
|
ENSP00000262367.5:p.Asn1425His
|
|
ENST00000262367.9:c.4273A>C
|
ENSP00000262367.5:p.Asn1425His
|
|
ENST00000382070.7:c.4159A>C
|
ENSP00000371502.3:p.Asn1387His
|
|
ENST00000570939.2:c.2908A>C
|
ENSP00000461002.2:p.Asn970His
|
|
ENST00000573517.6:c.579A>C
|
|
|
ENST00000574740.1:n.215+814A>C
|
|
|
ENST00000576720.1:n.3210A>C
|
|
|
NM_001079846.1:c.4159A>C
|
NP_001073315.1:p.Asn1387His
|
|
NM_004380.2:c.4273A>C
|
NP_004371.2:p.Asn1425His
|
|
XM_005255124.3:c.4228A>C
|
XP_005255181.1:p.Asn1410His
|
|
XM_005255125.3:c.3856A>C
|
XP_005255182.1:p.Asn1286His
|
|
XM_006720848.2:c.4133+814A>C
|
XP_006720911.1:n.4133+814A>C
|
|
XM_011522380.1:c.4219A>C
|
XP_011520682.1:p.Asn1407His
|
|
XM_011522381.1:c.3520A>C
|
XP_011520683.1:p.Asn1174His
|
|
XM_005255124.4:c.4228A>C
|
XP_005255181.1:p.Asn1410His
|
|
XM_005255125.4:c.3856A>C
|
XP_005255182.1:p.Asn1286His
|
|
XM_006720848.3:c.4133+814A>C
|
XP_006720911.1:n.4133+814A>C
|
|
XM_011522381.2:c.3520A>C
|
XP_011520683.1:p.Asn1174His
|
|
XM_017022944.1:c.4267A>C
|
XP_016878433.1:p.Asn1423His
|
|
NM_004380.3:c.4273A>C
MANE Select
|
NP_004371.2:p.Asn1425His
|
|