| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_015113.3 | 8913 | Missense Mutation | CTT,GTT | L2929V | NP_055928.3 |
| XM_005256561.2 | 8913 | Missense Mutation | CTT,GTT | L2930V | XP_005256618.1 |
| XM_011523759.2 | 8913 | Intron | XP_011522061.1 | ||
| XM_017024382.1 | 8913 | Missense Mutation | CTT,GTT | L2930V | XP_016879871.1 |
| XM_017024383.1 | 8913 | Missense Mutation | CTT,GTT | L2929V | XP_016879872.1 |
| XM_017024384.1 | 8913 | Missense Mutation | CTT,GTT | L1545V | XP_016879873.1 |