Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001277127.1 | 1387 | UTR 3 | NP_001264056.1 | ||
NM_001277128.1 | 1387 | Missense Mutation | CCT,CTT | P457L | NP_001264057.1 |
NM_024727.3 | 1387 | Missense Mutation | CCT,CTT | P513L | NP_079003.2 |
XM_011513158.2 | 1387 | Missense Mutation | CCT,CTT | P457L | XP_011511460.1 |
XM_011513159.2 | 1387 | Missense Mutation | CCT,CTT | P457L | XP_011511461.1 |
XM_011513160.2 | 1387 | Intron | XP_011511462.1 | ||
XM_017007204.1 | 1387 | Missense Mutation | CCT,CTT | P448L | XP_016862693.1 |