| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001033925.1 | 1635 | Missense Mutation | CCT,TCT | P354S | NP_001029097.1 |
| NM_001323964.1 | 1635 | Missense Mutation | CCT,TCT | P214S | NP_001310893.1 |
| NM_001323965.1 | 1635 | Missense Mutation | CCT,TCT | P214S | NP_001310894.1 |
| NM_001323967.1 | 1635 | Missense Mutation | CCT,TCT | P214S | NP_001310896.1 |
| NM_001323968.1 | 1635 | Missense Mutation | CCT,TCT | P322S | NP_001310897.1 |
| NM_001323969.1 | 1635 | Missense Mutation | CCT,TCT | P298S | NP_001310898.1 |
| NM_001323970.1 | 1635 | Missense Mutation | CCT,TCT | P315S | NP_001310899.1 |
| NM_003252.3 | 1635 | Missense Mutation | CCT,TCT | P337S | NP_003243.1 |
| XM_017016605.1 | 1635 | Intron | XP_016872094.1 | ||
| XM_017016606.1 | 1635 | Missense Mutation | CCT,TCT | P214S | XP_016872095.1 |