Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001167595.1 | 1076 | Missense Mutation | CCT,CTT | P327L | NP_001161067.1 |
NM_014324.5 | 1076 | Missense Mutation | CCT,CTT | P327L | NP_055139.4 |
NM_203382.2 | 1076 | UTR 3 | NP_976316.1 |