ENST00000262367.10:c.6976C>G
MANE Select
|
ENSP00000262367.5:p.Gln2326Glu
|
|
ENST00000262367.9:c.6976C>G
|
ENSP00000262367.5:p.Gln2326Glu
|
|
ENST00000382070.7:c.6862C>G
|
ENSP00000371502.3:p.Gln2288Glu
|
|
NM_001079846.1:c.6862C>G
|
NP_001073315.1:p.Gln2288Glu
|
|
NM_004380.2:c.6976C>G
|
NP_004371.2:p.Gln2326Glu
|
|
XM_005255124.3:c.6931C>G
|
XP_005255181.1:p.Gln2311Glu
|
|
XM_005255125.3:c.6559C>G
|
XP_005255182.1:p.Gln2187Glu
|
|
XM_006720848.2:c.6715C>G
|
XP_006720911.1:p.Gln2239Glu
|
|
XM_011522380.1:c.6922C>G
|
XP_011520682.1:p.Gln2308Glu
|
|
XM_011522381.1:c.6223C>G
|
XP_011520683.1:p.Gln2075Glu
|
|
XM_005255124.4:c.6931C>G
|
XP_005255181.1:p.Gln2311Glu
|
|
XM_005255125.4:c.6559C>G
|
XP_005255182.1:p.Gln2187Glu
|
|
XM_006720848.3:c.6715C>G
|
XP_006720911.1:p.Gln2239Glu
|
|
XM_011522381.2:c.6223C>G
|
XP_011520683.1:p.Gln2075Glu
|
|
XM_017022944.1:c.6970C>G
|
XP_016878433.1:p.Gln2324Glu
|
|
NM_004380.3:c.6976C>G
MANE Select
|
NP_004371.2:p.Gln2326Glu
|
|