| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001177963.1 | 189 | Silent Mutation | CTG,GTG | L21V | NP_001171434.1 |
| NM_002431.3 | 189 | Silent Mutation | CTG,GTG | L21V | NP_002422.1 |
| XM_005267687.2 | 189 | Missense Mutation | CTG,GTG | L21V | XP_005267744.1 |
| XM_005267688.2 | 189 | Missense Mutation | CTG,GTG | L21V | XP_005267745.1 |
| XM_017021332.1 | 189 | Intron | XP_016876821.1 | ||
| XM_017021333.1 | 189 | UTR 5 | XP_016876822.1 | ||
| XM_017021334.1 | 189 | Intron | XP_016876823.1 |