| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001261408.1 | 2089 | Missense Mutation | AAC,AGC | N733S | NP_001248337.1 |
| NM_001261409.1 | 2089 | Missense Mutation | AAC,AGC | N733S | NP_001248338.1 |
| NM_001261410.1 | 2089 | Missense Mutation | AAC,AGC | N642S | NP_001248339.1 |
| NM_001308251.1 | 2089 | Missense Mutation | AAC,AGC | N409S | NP_001295180.1 |
| NM_003567.3 | 2089 | Missense Mutation | AAC,AGC | N733S | NP_003558.1 |
| XM_011542251.2 | 2089 | Missense Mutation | AAC,AGC | N513S | XP_011540553.1 |
| XM_017002480.1 | 2089 | Missense Mutation | AAC,AGC | N733S | XP_016857969.1 |
| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001024948.2 | 2089 | Intron | NP_001020119.1 | ||
| NM_001164473.2 | 2089 | Intron | NP_001157945.1 | ||
| NM_017737.4 | 2089 | Intron | NP_060207.2 | ||
| XM_011541625.2 | 2089 | Intron | XP_011539927.1 | ||
| XM_017001533.1 | 2089 | Intron | XP_016857022.1 |