Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000806.5 | 440 | Missense Mutation | CCG,TCG | P29S | NP_000797.2 |
NM_001127643.1 | 440 | Missense Mutation | CCG,TCG | P29S | NP_001121115.1 |
NM_001127644.1 | 440 | Missense Mutation | CCG,TCG | P29S | NP_001121116.1 |
NM_001127645.1 | 440 | Missense Mutation | CCG,TCG | P29S | NP_001121117.1 |
NM_001127648.1 | 440 | Missense Mutation | CCG,TCG | P29S | NP_001121120.1 |