Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001319953.1 | 411 | Intron | NP_001306882.1 | ||
NM_153007.4 | 411 | Missense Mutation | CGC,TGC | R77C | NP_694552.2 |
XM_005256476.3 | 411 | Intron | XP_005256533.1 | ||
XM_011523688.1 | 411 | Intron | XP_011521990.1 |