Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001163484.1 | 1125 | Missense Mutation | CCT,CTT | P132L | NP_001156956.1 |
NM_025230.4 | 1125 | Missense Mutation | CCT,CTT | P132L | NP_079506.3 |
NM_181357.2 | 1125 | Missense Mutation | CCT,CTT | P106L | NP_852002.1 |