| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_020935.2 | 3279 | Missense Mutation | AGC,CGC | S968R | NP_065986.2 |
| XM_005246720.2 | 3279 | Missense Mutation | AGC,CGC | S968R | XP_005246777.1 |
| XM_005246721.3 | 3279 | Missense Mutation | AGC,CGC | S968R | XP_005246778.1 |
| XM_005246722.3 | 3279 | Missense Mutation | AGC,CGC | S968R | XP_005246779.1 |
| XM_005246724.1 | 3279 | Missense Mutation | AGC,CGC | S946R | XP_005246781.1 |
| XM_011511538.2 | 3279 | Missense Mutation | AGC,CGC | S968R | XP_011509840.1 |
| XM_011511541.2 | 3279 | Intron | XP_011509843.1 | ||
| XM_017004577.1 | 3279 | Missense Mutation | AGC,CGC | S720R | XP_016860066.1 |