ENST00000262367.10:c.4447A>G
MANE Select
|
ENSP00000262367.5:p.Ile1483Val
|
|
ENST00000262367.9:c.4447A>G
|
ENSP00000262367.5:p.Ile1483Val
|
|
ENST00000382070.7:c.4333A>G
|
ENSP00000371502.3:p.Ile1445Val
|
|
ENST00000570939.2:c.3082A>G
|
ENSP00000461002.2:p.Ile1028Val
|
|
ENST00000571763.5:n.237A>G
|
|
|
ENST00000574740.1:n.268A>G
|
|
|
ENST00000576720.1:n.3270A>G
|
|
|
NM_001079846.1:c.4333A>G
|
NP_001073315.1:p.Ile1445Val
|
|
NM_004380.2:c.4447A>G
|
NP_004371.2:p.Ile1483Val
|
|
XM_005255124.3:c.4402A>G
|
XP_005255181.1:p.Ile1468Val
|
|
XM_005255125.3:c.4030A>G
|
XP_005255182.1:p.Ile1344Val
|
|
XM_006720848.2:c.4186A>G
|
XP_006720911.1:p.Ile1396Val
|
|
XM_011522380.1:c.4393A>G
|
XP_011520682.1:p.Ile1465Val
|
|
XM_011522381.1:c.3694A>G
|
XP_011520683.1:p.Ile1232Val
|
|
XM_005255124.4:c.4402A>G
|
XP_005255181.1:p.Ile1468Val
|
|
XM_005255125.4:c.4030A>G
|
XP_005255182.1:p.Ile1344Val
|
|
XM_006720848.3:c.4186A>G
|
XP_006720911.1:p.Ile1396Val
|
|
XM_011522381.2:c.3694A>G
|
XP_011520683.1:p.Ile1232Val
|
|
XM_017022944.1:c.4441A>G
|
XP_016878433.1:p.Ile1481Val
|
|
NM_004380.3:c.4447A>G
MANE Select
|
NP_004371.2:p.Ile1483Val
|
|