ENST00000262367.10:c.5554C>G
MANE Select
|
ENSP00000262367.5:p.Gln1852Glu
|
|
ENST00000262367.9:c.5554C>G
|
ENSP00000262367.5:p.Gln1852Glu
|
|
ENST00000382070.7:c.5440C>G
|
ENSP00000371502.3:p.Gln1814Glu
|
|
NM_001079846.1:c.5440C>G
|
NP_001073315.1:p.Gln1814Glu
|
|
NM_004380.2:c.5554C>G
|
NP_004371.2:p.Gln1852Glu
|
|
XM_005255124.3:c.5509C>G
|
XP_005255181.1:p.Gln1837Glu
|
|
XM_005255125.3:c.5137C>G
|
XP_005255182.1:p.Gln1713Glu
|
|
XM_006720848.2:c.5293C>G
|
XP_006720911.1:p.Gln1765Glu
|
|
XM_011522380.1:c.5500C>G
|
XP_011520682.1:p.Gln1834Glu
|
|
XM_011522381.1:c.4801C>G
|
XP_011520683.1:p.Gln1601Glu
|
|
XM_005255124.4:c.5509C>G
|
XP_005255181.1:p.Gln1837Glu
|
|
XM_005255125.4:c.5137C>G
|
XP_005255182.1:p.Gln1713Glu
|
|
XM_006720848.3:c.5293C>G
|
XP_006720911.1:p.Gln1765Glu
|
|
XM_011522381.2:c.4801C>G
|
XP_011520683.1:p.Gln1601Glu
|
|
XM_017022944.1:c.5548C>G
|
XP_016878433.1:p.Gln1850Glu
|
|
NM_004380.3:c.5554C>G
MANE Select
|
NP_004371.2:p.Gln1852Glu
|
|