ENST00000262367.10:c.5175C>T
MANE Select
|
ENSP00000262367.5:p.Asp1725=
|
|
ENST00000262367.9:c.5175C>T
|
ENSP00000262367.5:p.Asp1725=
|
|
ENST00000382070.7:c.5061C>T
|
ENSP00000371502.3:p.Asp1687=
|
|
NM_001079846.1:c.5061C>T
|
NP_001073315.1:p.Asp1687=
|
|
NM_004380.2:c.5175C>T
|
NP_004371.2:p.Asp1725=
|
|
XM_005255124.3:c.5130C>T
|
XP_005255181.1:p.Asp1710=
|
|
XM_005255125.3:c.4758C>T
|
XP_005255182.1:p.Asp1586=
|
|
XM_006720848.2:c.4914C>T
|
XP_006720911.1:p.Asp1638=
|
|
XM_011522380.1:c.5121C>T
|
XP_011520682.1:p.Asp1707=
|
|
XM_011522381.1:c.4422C>T
|
XP_011520683.1:p.Asp1474=
|
|
XM_005255124.4:c.5130C>T
|
XP_005255181.1:p.Asp1710=
|
|
XM_005255125.4:c.4758C>T
|
XP_005255182.1:p.Asp1586=
|
|
XM_006720848.3:c.4914C>T
|
XP_006720911.1:p.Asp1638=
|
|
XM_011522381.2:c.4422C>T
|
XP_011520683.1:p.Asp1474=
|
|
XM_017022944.1:c.5169C>T
|
XP_016878433.1:p.Asp1723=
|
|
NM_004380.3:c.5175C>T
MANE Select
|
NP_004371.2:p.Asp1725=
|
|