|
ENST00000267868.8:c.499A>G
MANE Select
|
ENSP00000267868.3:p.Arg167Gly
|
|
|
ENST00000532743.6:c.499A>G
|
ENSP00000433924.2:p.Arg167Gly
|
|
|
ENST00000645673.2:c.502A>G
|
ENSP00000493712.2:p.Arg168Gly
|
|
|
ENST00000267868.7:c.499A>G
|
ENSP00000267868.3:p.Arg167Gly
|
|
|
ENST00000382643.7:c.502A>G
|
ENSP00000372088.3:p.Arg168Gly
|
|
|
ENST00000423169.6:c.499A>G
|
ENSP00000406602.2:p.Arg167Gly
|
|
|
ENST00000525066.5:c.435+9752A>G
|
ENSP00000431864.1:n.435+9752A>G
|
|
|
ENST00000527860.5:c.499A>G
|
ENSP00000432759.1:p.Arg167Gly
|
|
|
ENST00000531277.2:c.*78A>G
|
ENSP00000436512.2:n.*78A>G
|
|
|
ENST00000532743.5:c.502A>G
|
ENSP00000433924.1:p.Arg168Gly
|
|
|
ENST00000557850.5:c.226-18A>G
|
ENSP00000454176.1:n.226-18A>G
|
|
|
NM_001164269.1:c.502A>G
|
NP_001157741.1:p.Arg168Gly
|
|
|
NM_001164270.1:c.499A>G
|
NP_001157742.1:p.Arg167Gly
|
|
|
NM_002875.4:c.499A>G
|
NP_002866.2:p.Arg167Gly
|
|
|
NM_133487.3:c.502A>G
|
NP_597994.3:p.Arg168Gly
|
|
|
XM_006720626.2:c.499A>G
|
XP_006720689.1:p.Arg167Gly
|
|
|
XM_011521857.1:c.499A>G
|
XP_011520159.1:p.Arg167Gly
|
|
|
XM_011521858.1:c.499A>G
|
XP_011520160.1:p.Arg167Gly
|
|
|
XM_011521859.1:c.499A>G
|
XP_011520161.1:p.Arg167Gly
|
|
|
XM_011521860.1:c.499A>G
|
XP_011520162.1:p.Arg167Gly
|
|
|
XM_011521861.1:c.499A>G
|
XP_011520163.1:p.Arg167Gly
|
|
|
XM_011521862.1:c.127A>G
|
XP_011520164.1:p.Arg43Gly
|
|
|
XM_006720626.3:c.499A>G
|
XP_006720689.1:p.Arg167Gly
|
|
|
XM_011521857.2:c.499A>G
|
XP_011520159.1:p.Arg167Gly
|
|
|
XM_011521858.2:c.499A>G
|
XP_011520160.1:p.Arg167Gly
|
|
|
XM_011521859.2:c.499A>G
|
XP_011520161.1:p.Arg167Gly
|
|
|
XM_011521860.2:c.499A>G
|
XP_011520162.1:p.Arg167Gly
|
|
|
XM_011521861.2:c.499A>G
|
XP_011520163.1:p.Arg167Gly
|
|
|
XM_011521862.3:c.127A>G
|
XP_011520164.1:p.Arg43Gly
|
|
|
NM_001164269.2:c.502A>G
|
NP_001157741.1:p.Arg168Gly
|
|
|
NM_001164270.2:c.499A>G
|
NP_001157742.1:p.Arg167Gly
|
|
|
NM_002875.5:c.499A>G
MANE Select
|
NP_002866.2:p.Arg167Gly
|
|
|
NM_133487.4:c.502A>G
|
NP_597994.3:p.Arg168Gly
|
|
