| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002269.2 | 347 | Missense Mutation | CCA,GCA | P79A | NP_002260.2 |
| XM_011535805.1 | 347 | Missense Mutation | CCA,GCA | P99A | XP_011534107.1 |
| XM_017010838.1 | 347 | Missense Mutation | CCA,GCA | P99A | XP_016866327.1 |
| XM_017010839.1 | 347 | Missense Mutation | CCA,GCA | P79A | XP_016866328.1 |
| XM_017010840.1 | 347 | Missense Mutation | CCA,GCA | P76A | XP_016866329.1 |
| XM_017010841.1 | 347 | Intron | XP_016866330.1 | ||
| XM_017010842.1 | 347 | UTR 5 | XP_016866331.1 | ||
| XM_017010843.1 | 347 | UTR 5 | XP_016866332.1 |