Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_033125.3 | 1235 | Missense Mutation | CCC,CTC | P555L | NP_149116.2 |
XM_005267184.3 | 1235 | Missense Mutation | CCC,CTC | P385L | XP_005267241.1 |
XM_011536204.2 | 1235 | Missense Mutation | CCC,CTC | P512L | XP_011534506.1 |
XM_011536205.2 | 1235 | UTR 3 | XP_011534507.1 | ||
XM_011536206.2 | 1235 | Missense Mutation | CCC,CTC | P461L | XP_011534508.1 |
XM_011536207.2 | 1235 | Missense Mutation | CCC,CTC | P437L | XP_011534509.1 |
XM_011536208.2 | 1235 | Missense Mutation | CCC,CTC | P425L | XP_011534510.1 |
XM_011536209.2 | 1235 | Missense Mutation | CCC,CTC | P420L | XP_011534511.1 |
XM_011536210.1 | 1235 | Intron | XP_011534512.1 | ||
XM_011536211.2 | 1235 | Missense Mutation | CCC,CTC | P395L | XP_011534513.1 |
XM_011536212.2 | 1235 | Missense Mutation | CCC,CTC | P325L | XP_011534514.1 |