| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001286398.2 | 377 | Missense Mutation | AGC,ATC | S81I | NP_001273327.1 |
| NM_152553.4 | 377 | Intron | NP_689766.1 | ||
| XM_011535494.2 | 377 | Missense Mutation | AGC,ATC | S81I | XP_011533796.1 |
| XM_011535495.2 | 377 | Missense Mutation | AGC,ATC | S81I | XP_011533797.1 |
| XM_011535496.2 | 377 | Missense Mutation | AGC,ATC | S81I | XP_011533798.1 |
| XM_011535499.2 | 377 | Missense Mutation | AGC,ATC | S81I | XP_011533801.1 |
| XM_011535500.2 | 377 | Intron | XP_011533802.1 | ||
| XM_017010317.1 | 377 | Missense Mutation | AGC,ATC | S81I | XP_016865806.1 |