| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001301016.2 | 409 | Intron | NP_001287945.1 | ||
| NM_001321208.1 | 409 | UTR 5 | NP_001308137.1 | ||
| NM_001321211.1 | 409 | Intron | NP_001308140.1 | ||
| NM_007040.5 | 409 | Missense Mutation | ACC,GCC | T27A | NP_008971.2 |
| NM_144732.4 | 409 | Intron | NP_653333.1 | ||
| XM_005258459.3 | 409 | Missense Mutation | ACC,GCC | T27A | XP_005258516.1 |
| XM_005258461.4 | 409 | Intron | XP_005258518.1 | ||
| XM_005258463.3 | 409 | UTR 5 | XP_005258520.1 | ||
| XM_005258464.3 | 409 | Intron | XP_005258521.1 | ||
| XM_005258465.4 | 409 | Intron | XP_005258522.1 | ||
| XM_011526392.2 | 409 | Missense Mutation | ACC,GCC | T27A | XP_011524694.1 |
| XM_011526393.2 | 409 | Intron | XP_011524695.1 | ||
| XM_011526394.2 | 409 | Intron | XP_011524696.1 | ||
| XM_011526395.2 | 409 | Intron | XP_011524697.1 |