| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002848.3 | 501 | Missense Mutation | GCC,TCC | A11S | NP_002839.1 |
| NM_030667.2 | 501 | Missense Mutation | GCC,TCC | A11S | NP_109592.1 |
| NM_030668.2 | 501 | Intron | NP_109593.1 | ||
| NM_030669.2 | 501 | Intron | NP_109594.1 | ||
| NM_030670.2 | 501 | Intron | NP_109595.1 | ||
| NM_030671.2 | 501 | Intron | NP_109596.1 | ||
| XM_017019725.1 | 501 | Missense Mutation | GCC,TCC | A11S | XP_016875214.1 |