Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
XM_005269101.1 | 3377 | Missense Mutation | CCT,GCT | P1144A | XP_005269158.1 |
XM_005269102.1 | 3377 | Missense Mutation | CCT,GCT | P1143A | XP_005269159.1 |
XM_005269103.1 | 3377 | Missense Mutation | CCT,GCT | P1112A | XP_005269160.1 |
XM_005269104.1 | 3377 | Intron | XP_005269161.1 | ||
XM_011538693.2 | 3377 | Missense Mutation | CCT,GCT | P893A | XP_011536995.1 |
XM_017019884.1 | 3377 | Intron | XP_016875373.1 | ||
XM_017019885.1 | 3377 | Intron | XP_016875374.1 | ||
XM_017019886.1 | 3377 | Intron | XP_016875375.1 | ||
XM_017019887.1 | 3377 | Missense Mutation | CCT,GCT | P862A | XP_016875376.1 |