ENST00000262367.10:c.5326A>T
MANE Select
|
ENSP00000262367.5:p.Ile1776Phe
|
|
ENST00000262367.9:c.5326A>T
|
ENSP00000262367.5:p.Ile1776Phe
|
|
ENST00000382070.7:c.5212A>T
|
ENSP00000371502.3:p.Ile1738Phe
|
|
NM_001079846.1:c.5212A>T
|
NP_001073315.1:p.Ile1738Phe
|
|
NM_004380.2:c.5326A>T
|
NP_004371.2:p.Ile1776Phe
|
|
XM_005255124.3:c.5281A>T
|
XP_005255181.1:p.Ile1761Phe
|
|
XM_005255125.3:c.4909A>T
|
XP_005255182.1:p.Ile1637Phe
|
|
XM_006720848.2:c.5065A>T
|
XP_006720911.1:p.Ile1689Phe
|
|
XM_011522380.1:c.5272A>T
|
XP_011520682.1:p.Ile1758Phe
|
|
XM_011522381.1:c.4573A>T
|
XP_011520683.1:p.Ile1525Phe
|
|
XM_005255124.4:c.5281A>T
|
XP_005255181.1:p.Ile1761Phe
|
|
XM_005255125.4:c.4909A>T
|
XP_005255182.1:p.Ile1637Phe
|
|
XM_006720848.3:c.5065A>T
|
XP_006720911.1:p.Ile1689Phe
|
|
XM_011522381.2:c.4573A>T
|
XP_011520683.1:p.Ile1525Phe
|
|
XM_017022944.1:c.5320A>T
|
XP_016878433.1:p.Ile1774Phe
|
|
NM_004380.3:c.5326A>T
MANE Select
|
NP_004371.2:p.Ile1776Phe
|
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