| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001303228.1 | 986 | Missense Mutation | ACG,ATG | T277M | NP_001290157.1 |
| NM_024943.2 | 986 | Missense Mutation | ACG,ATG | T278M | NP_079219.1 |
| XM_005262670.3 | 986 | Intron | XP_005262727.1 | ||
| XM_011513749.2 | 986 | Missense Mutation | ACG,ATG | T278M | XP_011512051.1 |
| XM_011513750.2 | 986 | Missense Mutation | ACG,ATG | T277M | XP_011512052.1 |
| XM_011513751.2 | 986 | Intron | XP_011512053.1 | ||
| XM_011513752.2 | 986 | Intron | XP_011512054.1 | ||
| XM_011513753.2 | 986 | Missense Mutation | ACG,ATG | T250M | XP_011512055.1 |
| XM_011513754.2 | 986 | Missense Mutation | ACG,ATG | T208M | XP_011512056.1 |
| XM_017008629.1 | 986 | Missense Mutation | ACG,ATG | T208M | XP_016864118.1 |