| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001324171.1 | 2725 | Intron | NP_001311100.1 | ||
| NM_001324172.1 | 2725 | Intron | NP_001311101.1 | ||
| NM_030581.3 | 2725 | Missense Mutation | CCC,TCC | P961S | NP_085058.3 |
| XM_005256146.3 | 2725 | Missense Mutation | CCC,TCC | P980S | XP_005256203.1 |
| XM_011523331.2 | 2725 | Missense Mutation | CCC,TCC | P673S | XP_011521633.1 |
| XM_011523332.2 | 2725 | Missense Mutation | CCC,TCC | P659S | XP_011521634.1 |
| XM_017023667.1 | 2725 | Missense Mutation | CCC,TCC | P709S | XP_016879156.1 |
| XM_017023668.1 | 2725 | Missense Mutation | CCC,TCC | P709S | XP_016879157.1 |
| XM_017023669.1 | 2725 | Missense Mutation | CCC,TCC | P673S | XP_016879158.1 |
| XM_017023670.1 | 2725 | Missense Mutation | CCC,TCC | P659S | XP_016879159.1 |