| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001178100.1 | 637 | Missense Mutation | TGC,TTC | C193F | NP_001171571.1 |
| NM_004931.4 | 637 | Intron | NP_004922.1 | ||
| NM_172101.3 | 637 | UTR 3 | NP_742099.1 | ||
| NM_172102.3 | 637 | Silent Mutation | CTG,CTT | L205L | NP_742100.1 |
| NM_172213.3 | 637 | Silent Mutation | CTG,CTT | L235L | NP_757362.1 |
| XM_011533164.2 | 637 | Intron | XP_011531466.1 |