| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001301062.1 | 438 | UTR 5 | NP_001287991.1 | ||
| NM_153608.2 | 438 | Missense Mutation | CGC,CTC | R30L | NP_705836.1 |
| XM_011526574.2 | 438 | Missense Mutation | CGC,CTC | R76L | XP_011524876.1 |
| XM_017026414.1 | 438 | Missense Mutation | CGC,CTC | R76L | XP_016881903.1 |
| XM_017026415.1 | 438 | Missense Mutation | CGC,CTC | R30L | XP_016881904.1 |