ENST00000262367.10:c.4543A>G
MANE Select
|
ENSP00000262367.5:p.Ile1515Val
|
|
ENST00000262367.9:c.4543A>G
|
ENSP00000262367.5:p.Ile1515Val
|
|
ENST00000382070.7:c.4429A>G
|
ENSP00000371502.3:p.Ile1477Val
|
|
ENST00000570939.2:c.3178A>G
|
ENSP00000461002.2:p.Ile1060Val
|
|
ENST00000571763.5:n.333A>G
|
|
|
ENST00000574740.1:n.364A>G
|
|
|
ENST00000576720.1:n.3366A>G
|
|
|
NM_001079846.1:c.4429A>G
|
NP_001073315.1:p.Ile1477Val
|
|
NM_004380.2:c.4543A>G
|
NP_004371.2:p.Ile1515Val
|
|
XM_005255124.3:c.4498A>G
|
XP_005255181.1:p.Ile1500Val
|
|
XM_005255125.3:c.4126A>G
|
XP_005255182.1:p.Ile1376Val
|
|
XM_006720848.2:c.4282A>G
|
XP_006720911.1:p.Ile1428Val
|
|
XM_011522380.1:c.4489A>G
|
XP_011520682.1:p.Ile1497Val
|
|
XM_011522381.1:c.3790A>G
|
XP_011520683.1:p.Ile1264Val
|
|
XM_005255124.4:c.4498A>G
|
XP_005255181.1:p.Ile1500Val
|
|
XM_005255125.4:c.4126A>G
|
XP_005255182.1:p.Ile1376Val
|
|
XM_006720848.3:c.4282A>G
|
XP_006720911.1:p.Ile1428Val
|
|
XM_011522381.2:c.3790A>G
|
XP_011520683.1:p.Ile1264Val
|
|
XM_017022944.1:c.4537A>G
|
XP_016878433.1:p.Ile1513Val
|
|
NM_004380.3:c.4543A>G
MANE Select
|
NP_004371.2:p.Ile1515Val
|
|