ENST00000262367.10:c.5328C>G
MANE Select
|
ENSP00000262367.5:p.Ile1776Met
|
|
ENST00000262367.9:c.5328C>G
|
ENSP00000262367.5:p.Ile1776Met
|
|
ENST00000382070.7:c.5214C>G
|
ENSP00000371502.3:p.Ile1738Met
|
|
NM_001079846.1:c.5214C>G
|
NP_001073315.1:p.Ile1738Met
|
|
NM_004380.2:c.5328C>G
|
NP_004371.2:p.Ile1776Met
|
|
XM_005255124.3:c.5283C>G
|
XP_005255181.1:p.Ile1761Met
|
|
XM_005255125.3:c.4911C>G
|
XP_005255182.1:p.Ile1637Met
|
|
XM_006720848.2:c.5067C>G
|
XP_006720911.1:p.Ile1689Met
|
|
XM_011522380.1:c.5274C>G
|
XP_011520682.1:p.Ile1758Met
|
|
XM_011522381.1:c.4575C>G
|
XP_011520683.1:p.Ile1525Met
|
|
XM_005255124.4:c.5283C>G
|
XP_005255181.1:p.Ile1761Met
|
|
XM_005255125.4:c.4911C>G
|
XP_005255182.1:p.Ile1637Met
|
|
XM_006720848.3:c.5067C>G
|
XP_006720911.1:p.Ile1689Met
|
|
XM_011522381.2:c.4575C>G
|
XP_011520683.1:p.Ile1525Met
|
|
XM_017022944.1:c.5322C>G
|
XP_016878433.1:p.Ile1774Met
|
|
NM_004380.3:c.5328C>G
MANE Select
|
NP_004371.2:p.Ile1776Met
|
|