ENST00000262367.10:c.6146C>G
MANE Select
|
ENSP00000262367.5:p.Ala2049Gly
|
|
ENST00000262367.9:c.6146C>G
|
ENSP00000262367.5:p.Ala2049Gly
|
|
ENST00000382070.7:c.6032C>G
|
ENSP00000371502.3:p.Ala2011Gly
|
|
NM_001079846.1:c.6032C>G
|
NP_001073315.1:p.Ala2011Gly
|
|
NM_004380.2:c.6146C>G
|
NP_004371.2:p.Ala2049Gly
|
|
XM_005255124.3:c.6101C>G
|
XP_005255181.1:p.Ala2034Gly
|
|
XM_005255125.3:c.5729C>G
|
XP_005255182.1:p.Ala1910Gly
|
|
XM_006720848.2:c.5885C>G
|
XP_006720911.1:p.Ala1962Gly
|
|
XM_011522380.1:c.6092C>G
|
XP_011520682.1:p.Ala2031Gly
|
|
XM_011522381.1:c.5393C>G
|
XP_011520683.1:p.Ala1798Gly
|
|
XM_005255124.4:c.6101C>G
|
XP_005255181.1:p.Ala2034Gly
|
|
XM_005255125.4:c.5729C>G
|
XP_005255182.1:p.Ala1910Gly
|
|
XM_006720848.3:c.5885C>G
|
XP_006720911.1:p.Ala1962Gly
|
|
XM_011522381.2:c.5393C>G
|
XP_011520683.1:p.Ala1798Gly
|
|
XM_017022944.1:c.6140C>G
|
XP_016878433.1:p.Ala2047Gly
|
|
NM_004380.3:c.6146C>G
MANE Select
|
NP_004371.2:p.Ala2049Gly
|
|