Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001031735.2 | 489 | Missense Mutation | CGC,TGC | R131C | NP_001026905.2 |
NM_001039846.1 | 489 | Missense Mutation | CGC,TGC | R131C | NP_001034935.1 |
XM_005259480.3 | 489 | Missense Mutation | CGC,TGC | R131C | XP_005259537.2 |