ENST00000262367.10:c.4503G>T
MANE Select
|
ENSP00000262367.5:p.Glu1501Asp
|
|
ENST00000262367.9:c.4503G>T
|
ENSP00000262367.5:p.Glu1501Asp
|
|
ENST00000382070.7:c.4389G>T
|
ENSP00000371502.3:p.Glu1463Asp
|
|
ENST00000570939.2:c.3138G>T
|
ENSP00000461002.2:p.Glu1046Asp
|
|
ENST00000571763.5:n.293G>T
|
|
|
ENST00000574740.1:n.324G>T
|
|
|
ENST00000576720.1:n.3326G>T
|
|
|
NM_001079846.1:c.4389G>T
|
NP_001073315.1:p.Glu1463Asp
|
|
NM_004380.2:c.4503G>T
|
NP_004371.2:p.Glu1501Asp
|
|
XM_005255124.3:c.4458G>T
|
XP_005255181.1:p.Glu1486Asp
|
|
XM_005255125.3:c.4086G>T
|
XP_005255182.1:p.Glu1362Asp
|
|
XM_006720848.2:c.4242G>T
|
XP_006720911.1:p.Glu1414Asp
|
|
XM_011522380.1:c.4449G>T
|
XP_011520682.1:p.Glu1483Asp
|
|
XM_011522381.1:c.3750G>T
|
XP_011520683.1:p.Glu1250Asp
|
|
XM_005255124.4:c.4458G>T
|
XP_005255181.1:p.Glu1486Asp
|
|
XM_005255125.4:c.4086G>T
|
XP_005255182.1:p.Glu1362Asp
|
|
XM_006720848.3:c.4242G>T
|
XP_006720911.1:p.Glu1414Asp
|
|
XM_011522381.2:c.3750G>T
|
XP_011520683.1:p.Glu1250Asp
|
|
XM_017022944.1:c.4497G>T
|
XP_016878433.1:p.Glu1499Asp
|
|
NM_004380.3:c.4503G>T
MANE Select
|
NP_004371.2:p.Glu1501Asp
|
|