| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001012964.2 | 895 | Missense Mutation | CCT,TCT | P152S | NP_001012982.1 |
| NM_001012965.2 | 895 | Missense Mutation | CCT,TCT | P45S | NP_001012983.1 |
| NM_001319948.1 | 895 | Missense Mutation | CCT,TCT | P45S | NP_001306877.1 |
| NM_001319949.1 | 895 | Missense Mutation | CCT,TCT | P45S | NP_001306878.1 |
| NM_002774.3 | 895 | Missense Mutation | CCT,TCT | P152S | NP_002765.1 |