| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_014429.3 | 2998 | Missense Mutation | AAT,AGT | N955S | NP_055244.3 |
| XM_005247362.2 | 2998 | Missense Mutation | AAT,AGT | N985S | XP_005247419.1 |
| XM_011512691.1 | 2998 | Missense Mutation | AAT,AGT | N987S | XP_011510993.1 |
| XM_011512692.1 | 2998 | Missense Mutation | AAT,AGT | N957S | XP_011510994.1 |
| XM_011512693.1 | 2998 | Missense Mutation | AAT,AGT | N922S | XP_011510995.1 |
| XM_011512694.1 | 2998 | Missense Mutation | AAT,AGT | N888S | XP_011510996.1 |
| XM_011512696.2 | 2998 | Missense Mutation | AAT,AGT | N761S | XP_011510998.1 |
| XM_011512697.2 | 2998 | Missense Mutation | AAT,AGT | N736S | XP_011510999.1 |
| XM_017006169.1 | 2998 | Intron | XP_016861658.1 | ||
| XM_017006170.1 | 2998 | Missense Mutation | AAT,AGT | N706S | XP_016861659.1 |