| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001276282.3 | 613 | Missense Mutation | ACC,CCC | T78P | NP_001263211.1 |
| NM_207303.4 | 613 | Missense Mutation | ACC,CCC | T78P | NP_997186.1 |
| XM_011539587.1 | 613 | Missense Mutation | ACC,CCC | T78P | XP_011537889.1 |
| XM_011539588.2 | 613 | Intron | XP_011537890.1 | ||
| XM_011539589.2 | 613 | Missense Mutation | ACC,CCC | T78P | XP_011537891.1 |
| XM_011539590.2 | 613 | Intron | XP_011537892.1 | ||
| XM_011539591.2 | 613 | Intron | XP_011537893.1 | ||
| XM_017016035.1 | 613 | Missense Mutation | ACC,CCC | T78P | XP_016871524.1 |
| XM_017016036.1 | 613 | Missense Mutation | ACC,CCC | T78P | XP_016871525.1 |
| XM_017016037.1 | 613 | Intron | XP_016871526.1 | ||
| XM_017016038.1 | 613 | Intron | XP_016871527.1 | ||
| XM_017016039.1 | 613 | Intron | XP_016871528.1 | ||
| XM_017016040.1 | 613 | Intron | XP_016871529.1 |