| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001131028.1 | 338 | Missense Mutation | CGT,TGT | R14C | NP_001124500.1 |
| NM_031482.4 | 338 | Missense Mutation | CGT,TGT | R14C | NP_113670.1 |
| XM_005248610.4 | 338 | Missense Mutation | CGT,TGT | R14C | XP_005248667.1 |
| XM_005248611.4 | 338 | Intron | XP_005248668.1 | ||
| XM_005248612.3 | 338 | Missense Mutation | CGT,TGT | R14C | XP_005248669.1 |
| XM_011543660.2 | 338 | Intron | XP_011541962.1 | ||
| XM_011543661.2 | 338 | Intron | XP_011541963.1 | ||
| XM_017009944.1 | 338 | Missense Mutation | CGT,TGT | R14C | XP_016865433.1 |