Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001122646.2 | 385 | Missense Mutation | CGC,TGC | R645C | NP_001116118.2 |
NM_001172667.1 | 385 | Missense Mutation | CGC,TGC | R104C | NP_001166138.1 |
NM_016490.4 | 385 | Missense Mutation | CGC,TGC | R85C | NP_057574.2 |
XM_011511294.2 | 385 | Missense Mutation | CGC,TGC | R609C | XP_011509596.1 |
XM_011511297.2 | 385 | Intron | XP_011509599.1 | ||
XM_017004263.1 | 385 | Missense Mutation | CGC,TGC | R688C | XP_016859752.1 |
XM_017004264.1 | 385 | Missense Mutation | CGC,TGC | R675C | XP_016859753.1 |
XM_017004265.1 | 385 | Intron | XP_016859754.1 | ||
XM_017004266.1 | 385 | Missense Mutation | CGC,TGC | R111C | XP_016859755.1 |
XM_017004267.1 | 385 | Missense Mutation | CGC,TGC | R110C | XP_016859756.1 |
XM_017004268.1 | 385 | Missense Mutation | CGC,TGC | R85C | XP_016859757.1 |