| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001305105.1 | 412 | Intron | NP_001292034.1 | ||
| NM_001305108.1 | 412 | Intron | NP_001292037.1 | ||
| NM_017432.4 | 412 | Intron | NP_059128.2 | ||
| XM_005258998.4 | 412 | Missense Mutation | CCC,CTC | P86L | XP_005259055.1 |
| XM_006723244.3 | 412 | Missense Mutation | CCC,CTC | P86L | XP_006723307.1 |
| XM_011527033.1 | 412 | Intron | XP_011525335.1 | ||
| XM_011527034.2 | 412 | Missense Mutation | CCC,CTC | P86L | XP_011525336.1 |
| XM_011527035.1 | 412 | UTR 5 | XP_011525337.1 | ||
| XM_017026879.1 | 412 | Missense Mutation | CCC,CTC | P86L | XP_016882368.1 |
| XM_017026880.1 | 412 | Intron | XP_016882369.1 |