| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001291419.1 | 911 | Missense Mutation | CTT,GTT | L188V | NP_001278348.1 |
| NM_173506.6 | 911 | Missense Mutation | CTT,GTT | L223V | NP_775777.3 |
| XM_005258543.3 | 911 | Missense Mutation | CTT,GTT | L236V | XP_005258600.1 |
| XM_005278383.4 | 911 | Missense Mutation | CTT,GTT | L236V | XP_005278440.1 |
| XM_005278385.4 | 911 | Missense Mutation | CTT,GTT | L236V | XP_005278442.1 |
| XM_005278387.4 | 911 | Intron | XP_005278444.1 | ||
| XM_005278388.3 | 911 | Missense Mutation | CTT,GTT | L174V | XP_005278445.1 |
| XM_006723035.2 | 911 | Missense Mutation | CTT,GTT | L232V | XP_006723098.1 |
| XM_011526483.2 | 911 | Missense Mutation | CTT,GTT | L236V | XP_011524785.1 |
| XM_011526484.2 | 911 | Missense Mutation | CTT,GTT | L236V | XP_011524786.1 |