| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_012174.1 | 218 | Intron | NP_036306.1 | ||
| NM_153348.2 | 218 | Missense Mutation | AGC,GGC | S46G | NP_699179.2 |
| XM_005253867.2 | 218 | UTR 5 | XP_005253924.1 | ||
| XM_005253868.3 | 218 | Intron | XP_005253925.1 | ||
| XM_017019175.1 | 218 | Intron | XP_016874664.1 | ||
| XM_017019176.1 | 218 | Intron | XP_016874665.1 | ||
| XM_017019177.1 | 218 | Intron | XP_016874666.1 | ||
| XM_017019178.1 | 218 | Intron | XP_016874667.1 |