Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001290187.1 | 134 | Intron | NP_001277116.1 | ||
NM_032534.3 | 134 | UTR 5 | NP_115923.2 | ||
XM_011516636.2 | 134 | Missense Mutation | GGT,TGT | G9C | XP_011514938.1 |
XM_011516637.2 | 134 | Missense Mutation | GGT,TGT | G9C | XP_011514939.1 |
XM_011516638.2 | 134 | Missense Mutation | GGT,TGT | G9C | XP_011514940.1 |
XM_011516639.2 | 134 | Missense Mutation | GGT,TGT | G9C | XP_011514941.1 |
XM_011516640.2 | 134 | Missense Mutation | GGT,TGT | G9C | XP_011514942.1 |
XM_011516641.2 | 134 | Intron | XP_011514943.1 | ||
XM_011516642.2 | 134 | UTR 5 | XP_011514944.1 | ||
XM_011516643.2 | 134 | Intron | XP_011514945.1 |