ENST00000262367.10:c.4529C>A
MANE Select
|
ENSP00000262367.5:p.Ala1510Glu
|
|
ENST00000262367.9:c.4529C>A
|
ENSP00000262367.5:p.Ala1510Glu
|
|
ENST00000382070.7:c.4415C>A
|
ENSP00000371502.3:p.Ala1472Glu
|
|
ENST00000570939.2:c.3164C>A
|
ENSP00000461002.2:p.Ala1055Glu
|
|
ENST00000571763.5:n.319C>A
|
|
|
ENST00000574740.1:n.350C>A
|
|
|
ENST00000576720.1:n.3352C>A
|
|
|
NM_001079846.1:c.4415C>A
|
NP_001073315.1:p.Ala1472Glu
|
|
NM_004380.2:c.4529C>A
|
NP_004371.2:p.Ala1510Glu
|
|
XM_005255124.3:c.4484C>A
|
XP_005255181.1:p.Ala1495Glu
|
|
XM_005255125.3:c.4112C>A
|
XP_005255182.1:p.Ala1371Glu
|
|
XM_006720848.2:c.4268C>A
|
XP_006720911.1:p.Ala1423Glu
|
|
XM_011522380.1:c.4475C>A
|
XP_011520682.1:p.Ala1492Glu
|
|
XM_011522381.1:c.3776C>A
|
XP_011520683.1:p.Ala1259Glu
|
|
XM_005255124.4:c.4484C>A
|
XP_005255181.1:p.Ala1495Glu
|
|
XM_005255125.4:c.4112C>A
|
XP_005255182.1:p.Ala1371Glu
|
|
XM_006720848.3:c.4268C>A
|
XP_006720911.1:p.Ala1423Glu
|
|
XM_011522381.2:c.3776C>A
|
XP_011520683.1:p.Ala1259Glu
|
|
XM_017022944.1:c.4523C>A
|
XP_016878433.1:p.Ala1508Glu
|
|
NM_004380.3:c.4529C>A
MANE Select
|
NP_004371.2:p.Ala1510Glu
|
|