Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001014433.2 | 768 | Missense Mutation | CTT,GTT | L92V | NP_001014433.1 |
NM_001014837.1 | 768 | Missense Mutation | CTT,GTT | L50V | NP_001014837.1 |
NM_001014838.1 | 768 | Missense Mutation | CTT,GTT | L50V | NP_001014838.1 |
NM_001014840.1 | 768 | Missense Mutation | CTT,GTT | L73V | NP_001014840.1 |
NM_015921.2 | 768 | Missense Mutation | CTT,GTT | L50V | NP_057005.1 |