| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001039649.2 | 1738 | Intron | NP_001034738.1 | ||
| NM_001039650.2 | 1738 | Intron | NP_001034739.1 | ||
| NM_001142684.1 | 1738 | Missense Mutation | ACC,GCC | T372A | NP_001136156.1 |
| XM_005266593.3 | 1738 | Missense Mutation | ACC,GCC | T372A | XP_005266650.1 |
| XM_005266594.2 | 1738 | Missense Mutation | ACC,GCC | T372A | XP_005266651.1 |
| XM_006719894.2 | 1738 | Missense Mutation | ACC,GCC | T372A | XP_006719957.1 |
| XM_011535309.1 | 1738 | Missense Mutation | ACC,GCC | T399A | XP_011533611.1 |
| XM_011535310.1 | 1738 | Missense Mutation | ACC,GCC | T217A | XP_011533612.1 |
| XM_017020849.1 | 1738 | Missense Mutation | ACC,GCC | T190A | XP_016876338.1 |
| XM_017020850.1 | 1738 | Missense Mutation | ACC,GCC | T190A | XP_016876339.1 |
| XM_017020851.1 | 1738 | Intron | XP_016876340.1 |