| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001135934.1 | 2346 | Missense Mutation | ACT,CCT | T688P | NP_001129406.1 |
| NM_001135935.1 | 2346 | Missense Mutation | ACT,CCT | T718P | NP_001129407.1 |
| NM_001135936.1 | 2346 | Missense Mutation | ACT,CCT | T688P | NP_001129408.1 |
| NM_001286665.1 | 2346 | Missense Mutation | ACT,CCT | T718P | NP_001273594.1 |
| NM_001286666.1 | 2346 | Intron | NP_001273595.1 | ||
| NM_001286667.1 | 2346 | Intron | NP_001273596.1 | ||
| NM_006475.2 | 2346 | Missense Mutation | ACT,CCT | T745P | NP_006466.2 |
| XM_005266231.2 | 2346 | Missense Mutation | ACT,CCT | T745P | XP_005266288.1 |
| XM_005266232.2 | 2346 | Missense Mutation | ACT,CCT | T715P | XP_005266289.1 |
| XM_017020355.1 | 2346 | Missense Mutation | ACT,CCT | T745P | XP_016875844.1 |
| XM_017020356.1 | 2346 | Missense Mutation | ACT,CCT | T745P | XP_016875845.1 |