Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001142572.1 | 1087 | Missense Mutation | CCC,CTC | P316L | NP_001136044.1 |
NM_024804.2 | 1087 | Missense Mutation | CCC,CTC | P402L | NP_079080.2 |
XM_005273270.2 | 1087 | Missense Mutation | CCC,CTC | P279L | XP_005273327.1 |
XM_005273271.2 | 1087 | Missense Mutation | CCC,CTC | P279L | XP_005273328.1 |