| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_000591.3 | 757 | Missense Mutation | ACG,ATG | T122M | NP_000582.1 |
| NM_001040021.2 | 757 | Missense Mutation | ACG,ATG | T122M | NP_001035110.1 |
| NM_001174104.1 | 757 | Missense Mutation | ACG,ATG | T122M | NP_001167575.1 |
| NM_001174105.1 | 757 | Missense Mutation | ACG,ATG | T122M | NP_001167576.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001300980.1 | 757 | Intron | NP_001287909.1 | ||
| NM_001300982.1 | 757 | Intron | NP_001287911.1 | ||
| NM_018502.4 | 757 | Intron | NP_060972.3 | ||
| XM_005268477.1 | 757 | Intron | XP_005268534.1 | ||
| XM_011537663.2 | 757 | Intron | XP_011535965.1 | ||
| XM_011537665.2 | 757 | Intron | XP_011535967.1 | ||
| XM_011537668.2 | 757 | Intron | XP_011535970.1 | ||
| XM_017009617.1 | 757 | Intron | XP_016865106.1 | ||
| XM_017009618.1 | 757 | Intron | XP_016865107.1 | ||
| XM_017009619.1 | 757 | Intron | XP_016865108.1 | ||
| XM_017009620.1 | 757 | Intron | XP_016865109.1 |