| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001199917.1 | 200 | Intron | NP_001186846.1 | ||
| NM_001199918.1 | 200 | Intron | NP_001186847.1 | ||
| NM_001199919.1 | 200 | Intron | NP_001186848.1 | ||
| NM_015599.2 | 200 | Intron | NP_056414.1 | ||
| XM_017010935.1 | 200 | Intron | XP_016866424.1 | ||
| XM_017010936.1 | 200 | Intron | XP_016866425.1 | ||
| XM_017010937.1 | 200 | Intron | XP_016866426.1 | ||
| XM_017010938.1 | 200 | Intron | XP_016866427.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001322335.1 | 200 | UTR 5 | NP_001309264.1 | ||
| NM_001322336.1 | 200 | UTR 5 | NP_001309265.1 | ||
| NM_001322337.1 | 200 | UTR 5 | NP_001309266.1 | ||
| NM_001322339.1 | 200 | UTR 5 | NP_001309268.1 | ||
| NM_033411.4 | 200 | Missense Mutation | GCG,TCG | A50S | NP_219479.2 |
| XM_017010222.1 | 200 | UTR 5 | XP_016865711.1 | ||
| XM_017010223.1 | 200 | UTR 5 | XP_016865712.1 |