ENST00000262367.10:c.5563A>G
MANE Select
|
ENSP00000262367.5:p.Ile1855Val
|
|
ENST00000262367.9:c.5563A>G
|
ENSP00000262367.5:p.Ile1855Val
|
|
ENST00000382070.7:c.5449A>G
|
ENSP00000371502.3:p.Ile1817Val
|
|
NM_001079846.1:c.5449A>G
|
NP_001073315.1:p.Ile1817Val
|
|
NM_004380.2:c.5563A>G
|
NP_004371.2:p.Ile1855Val
|
|
XM_005255124.3:c.5518A>G
|
XP_005255181.1:p.Ile1840Val
|
|
XM_005255125.3:c.5146A>G
|
XP_005255182.1:p.Ile1716Val
|
|
XM_006720848.2:c.5302A>G
|
XP_006720911.1:p.Ile1768Val
|
|
XM_011522380.1:c.5509A>G
|
XP_011520682.1:p.Ile1837Val
|
|
XM_011522381.1:c.4810A>G
|
XP_011520683.1:p.Ile1604Val
|
|
XM_005255124.4:c.5518A>G
|
XP_005255181.1:p.Ile1840Val
|
|
XM_005255125.4:c.5146A>G
|
XP_005255182.1:p.Ile1716Val
|
|
XM_006720848.3:c.5302A>G
|
XP_006720911.1:p.Ile1768Val
|
|
XM_011522381.2:c.4810A>G
|
XP_011520683.1:p.Ile1604Val
|
|
XM_017022944.1:c.5557A>G
|
XP_016878433.1:p.Ile1853Val
|
|
NM_004380.3:c.5563A>G
MANE Select
|
NP_004371.2:p.Ile1855Val
|
|