ENST00000262367.10:c.4470T>C
MANE Select
|
ENSP00000262367.5:p.Asp1490=
|
|
ENST00000262367.9:c.4470T>C
|
ENSP00000262367.5:p.Asp1490=
|
|
ENST00000382070.7:c.4356T>C
|
ENSP00000371502.3:p.Asp1452=
|
|
ENST00000570939.2:c.3105T>C
|
ENSP00000461002.2:p.Asp1035=
|
|
ENST00000571763.5:n.260T>C
|
|
|
ENST00000574740.1:n.291T>C
|
|
|
ENST00000576720.1:n.3293T>C
|
|
|
NM_001079846.1:c.4356T>C
|
NP_001073315.1:p.Asp1452=
|
|
NM_004380.2:c.4470T>C
|
NP_004371.2:p.Asp1490=
|
|
XM_005255124.3:c.4425T>C
|
XP_005255181.1:p.Asp1475=
|
|
XM_005255125.3:c.4053T>C
|
XP_005255182.1:p.Asp1351=
|
|
XM_006720848.2:c.4209T>C
|
XP_006720911.1:p.Asp1403=
|
|
XM_011522380.1:c.4416T>C
|
XP_011520682.1:p.Asp1472=
|
|
XM_011522381.1:c.3717T>C
|
XP_011520683.1:p.Asp1239=
|
|
XM_005255124.4:c.4425T>C
|
XP_005255181.1:p.Asp1475=
|
|
XM_005255125.4:c.4053T>C
|
XP_005255182.1:p.Asp1351=
|
|
XM_006720848.3:c.4209T>C
|
XP_006720911.1:p.Asp1403=
|
|
XM_011522381.2:c.3717T>C
|
XP_011520683.1:p.Asp1239=
|
|
XM_017022944.1:c.4464T>C
|
XP_016878433.1:p.Asp1488=
|
|
NM_004380.3:c.4470T>C
MANE Select
|
NP_004371.2:p.Asp1490=
|
|