| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001080997.2 | 914 | Intron | NP_001074466.1 | ||
| NM_001270440.1 | 914 | Missense Mutation | AAC,AGC | N195S | NP_001257369.1 |
| NM_001270441.1 | 914 | Intron | NP_001257370.1 | ||
| NM_001270442.1 | 914 | Intron | NP_001257371.1 | ||
| NM_001270443.1 | 914 | Intron | NP_001257372.1 | ||
| NM_001270444.1 | 914 | Intron | NP_001257373.1 | ||
| NM_001270445.1 | 914 | Intron | NP_001257374.1 | ||
| NM_031429.2 | 914 | Intron | NP_113617.1 | ||
| XM_005260089.1 | 914 | Intron | XP_005260146.1 | ||
| XM_005260090.3 | 914 | Intron | XP_005260147.1 | ||
| XM_011528343.1 | 914 | Intron | XP_011526645.1 | ||
| XM_011528344.2 | 914 | Intron | XP_011526646.1 | ||
| XM_011528345.1 | 914 | Intron | XP_011526647.1 | ||
| XM_017027343.1 | 914 | Intron | XP_016882832.1 | ||
| XM_017027344.1 | 914 | Intron | XP_016882833.1 |