| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_002841.3 | 438 | Missense Mutation | CTC,TTC | L21F | NP_002832.3 |
| XM_005265353.3 | 438 | Missense Mutation | CTC,TTC | L21F | XP_005265410.1 |
| XM_017006961.1 | 438 | Missense Mutation | CTC,TTC | L21F | XP_016862450.1 |
| XM_017006962.1 | 438 | Intron | XP_016862451.1 | ||
| XM_017006963.1 | 438 | Missense Mutation | CTC,TTC | L21F | XP_016862452.1 |
| XM_017006964.1 | 438 | Intron | XP_016862453.1 |