| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000546.5 | 952 | Missense Mutation | CCC,CTC | P337L | NP_000537.3 |
| NM_001126112.2 | 952 | Missense Mutation | CCC,CTC | P337L | NP_001119584.1 |
| NM_001126113.2 | 952 | UTR 3 | NP_001119585.1 | ||
| NM_001126114.2 | 952 | UTR 3 | NP_001119586.1 | ||
| NM_001126115.1 | 952 | Missense Mutation | CCC,CTC | P205L | NP_001119587.1 |
| NM_001126116.1 | 952 | UTR 3 | NP_001119588.1 | ||
| NM_001126117.1 | 952 | UTR 3 | NP_001119589.1 | ||
| NM_001126118.1 | 952 | Missense Mutation | CCC,CTC | P298L | NP_001119590.1 |
| NM_001276695.1 | 952 | UTR 3 | NP_001263624.1 | ||
| NM_001276696.1 | 952 | UTR 3 | NP_001263625.1 | ||
| NM_001276697.1 | 952 | Missense Mutation | CCC,CTC | P178L | NP_001263626.1 |
| NM_001276698.1 | 952 | UTR 3 | NP_001263627.1 | ||
| NM_001276699.1 | 952 | UTR 3 | NP_001263628.1 | ||
| NM_001276760.1 | 952 | Missense Mutation | CCC,CTC | P298L | NP_001263689.1 |
| NM_001276761.1 | 952 | Missense Mutation | CCC,CTC | P298L | NP_001263690.1 |