ENST00000311604.8:c.949A>G
MANE Select
|
ENSP00000308383.4:p.Arg317Gly
|
|
ENST00000311604.7:c.949A>G
|
ENSP00000308383.3:p.Arg317Gly
|
|
ENST00000381775.5:c.1333A>G
|
ENSP00000371194.1:p.Arg445Gly
|
|
ENST00000405957.6:c.763A>G
|
ENSP00000383932.2:p.Arg255Gly
|
|
ENST00000406638.6:c.763A>G
|
ENSP00000384022.2:p.Arg255Gly
|
|
ENST00000472974.5:n.819A>G
|
|
|
ENST00000484895.5:n.426A>G
|
|
|
ENST00000485341.5:n.1445A>G
|
|
|
ENST00000612798.4:c.763A>G
|
ENSP00000484140.1:p.Arg255Gly
|
|
NM_001013253.1:c.763A>G
|
NP_001013271.1:p.Arg255Gly
|
|
NM_001013254.1:c.763A>G
|
NP_001013272.1:p.Arg255Gly
|
|
NM_001013255.1:c.763A>G
|
NP_001013273.1:p.Arg255Gly
|
|
NM_001242932.1:c.1333A>G
|
NP_001229861.1:p.Arg445Gly
|
|
NM_001289005.1:c.763A>G
|
NP_001275934.1:p.Arg255Gly
|
|
NM_002339.2:c.949A>G
|
NP_002330.1:p.Arg317Gly
|
|
NM_001013253.2:c.763A>G
|
NP_001013271.1:p.Arg255Gly
|
|
NM_002339.3:c.949A>G
MANE Select
|
NP_002330.1:p.Arg317Gly
|
|
NM_001242932.2:c.1333A>G
|
NP_001229861.1:p.Arg445Gly
|
|
NM_001289005.2:c.763A>G
|
NP_001275934.1:p.Arg255Gly
|
|