ENST00000460843.6:c.1403C>G
MANE Select
|
ENSP00000417980.1:p.Ala468Gly
|
|
ENST00000629335.2:c.1403C>G
|
ENSP00000490056.1:p.Ala468Gly
|
|
ENST00000636027.1:c.1289C>G
|
ENSP00000489961.1:p.Ala430Gly
|
|
ENST00000637161.1:c.1310C>G
|
ENSP00000490328.1:p.Ala437Gly
|
|
ENST00000637261.1:c.1443C>G
|
ENSP00000490815.1:n.1443C>G
|
|
ENST00000637977.1:c.1348C>G
|
|
|
ENST00000638071.1:c.1030C>G
|
|
|
ENST00000640639.1:c.572C>G
|
ENSP00000491823.1:p.Ala191Gly
|
|
ENST00000371394.6:c.*1138C>G
|
ENSP00000485945.1:n.*1138C>G
|
|
ENST00000460843.5:c.1403C>G
|
ENSP00000417980.1:p.Ala468Gly
|
|
ENST00000462484.5:c.1403C>G
|
ENSP00000417328.1:p.Ala468Gly
|
|
ENST00000462942.3:c.260C>G
|
ENSP00000436107.1:p.Ala87Gly
|
|
ENST00000465566.2:c.95C>G
|
ENSP00000486261.1:p.Ala32Gly
|
|
ENST00000629808.2:c.496C>G
|
|
|
NM_001145527.1:c.1403C>G
|
NP_001138999.1:p.Ala468Gly
|
|
NM_024757.4:c.1403C>G
|
NP_079033.4:p.Ala468Gly
|
|
XM_005266105.3:c.1394C>G
|
XP_005266162.1:p.Ala465Gly
|
|
XM_005266110.1:c.1310C>G
|
XP_005266167.1:p.Ala437Gly
|
|
XM_006717288.2:c.1385C>G
|
XP_006717351.1:p.Ala462Gly
|
|
XM_011519021.1:c.1412C>G
|
XP_011517323.1:p.Ala471Gly
|
|
XM_011519022.1:c.1409C>G
|
XP_011517324.1:p.Ala470Gly
|
|
XM_011519023.1:c.1391C>G
|
XP_011517325.1:p.Ala464Gly
|
|
XM_011519024.1:c.1334C>G
|
XP_011517326.1:p.Ala445Gly
|
|
XM_011519025.1:c.1310C>G
|
XP_011517327.1:p.Ala437Gly
|
|
XM_011519026.1:c.1412C>G
|
XP_011517328.1:p.Ala471Gly
|
|
XM_011519027.1:c.1412C>G
|
XP_011517329.1:p.Ala471Gly
|
|
XM_011519028.1:c.1412C>G
|
XP_011517330.1:p.Ala471Gly
|
|
XM_011519033.1:c.1391C>G
|
XP_011517335.1:p.Ala464Gly
|
|
NM_001354259.1:c.1310C>G
|
NP_001341188.1:p.Ala437Gly
|
|
NM_001354263.1:c.1382C>G
|
NP_001341192.1:p.Ala461Gly
|
|
NM_001354611.1:c.1403C>G
|
NP_001341540.1:p.Ala468Gly
|
|
NM_001354612.1:c.1310C>G
|
NP_001341541.1:p.Ala437Gly
|
|
XM_005266105.5:c.1394C>G
|
XP_005266162.1:p.Ala465Gly
|
|
XM_011519021.3:c.1412C>G
|
XP_011517323.1:p.Ala471Gly
|
|
XM_011519022.3:c.1409C>G
|
XP_011517324.1:p.Ala470Gly
|
|
XM_011519023.3:c.1391C>G
|
XP_011517325.1:p.Ala464Gly
|
|
XM_017015134.1:c.1388C>G
|
XP_016870623.1:p.Ala463Gly
|
|
XM_017015136.2:c.1304C>G
|
XP_016870625.1:p.Ala435Gly
|
|
XM_017015137.1:c.1289C>G
|
XP_016870626.1:p.Ala430Gly
|
|
XM_017015138.1:c.1289C>G
|
XP_016870627.1:p.Ala430Gly
|
|
XM_024447674.1:c.1232C>G
|
XP_024303442.1:p.Ala411Gly
|
|
XM_024447675.1:c.1310C>G
|
XP_024303443.1:p.Ala437Gly
|
|
XM_024447676.1:c.527C>G
|
XP_024303444.1:p.Ala176Gly
|
|
XM_024447677.1:c.527C>G
|
XP_024303445.1:p.Ala176Gly
|
|
XM_024447678.1:c.1310C>G
|
XP_024303446.1:p.Ala437Gly
|
|
XM_024447679.1:c.1310C>G
|
XP_024303447.1:p.Ala437Gly
|
|
XM_024447680.1:c.1289C>G
|
XP_024303448.1:p.Ala430Gly
|
|
NM_024757.5:c.1403C>G
MANE Select
|
NP_079033.4:p.Ala468Gly
|
|
NM_001145527.2:c.1403C>G
|
NP_001138999.1:p.Ala468Gly
|
|
NM_001354259.2:c.1310C>G
|
NP_001341188.1:p.Ala437Gly
|
|
NM_001354263.2:c.1382C>G
|
NP_001341192.1:p.Ala461Gly
|
|
NM_001354611.2:c.1403C>G
|
NP_001341540.1:p.Ala468Gly
|
|
NM_001354612.2:c.1310C>G
|
NP_001341541.1:p.Ala437Gly
|
|