| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199809.1 | 2877 | Missense Mutation | CCT,CTT | P850L | NP_001186738.1 |
| NM_001199811.1 | 2877 | Missense Mutation | CCT,CTT | P885L | NP_001186740.1 |
| NM_001199812.1 | 2877 | Missense Mutation | CCT,CTT | P879L | NP_001186741.1 |
| NM_015434.3 | 2877 | Missense Mutation | CCT,CTT | P899L | NP_056249.1 |
| XM_011509396.2 | 2877 | Missense Mutation | CCT,CTT | P935L | XP_011507698.1 |
| XM_017000962.1 | 2877 | Intron | XP_016856451.1 |