Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_153453.1 | 438 | Intron | NP_703154.1 | ||
NM_182645.3 | 438 | Missense Mutation | CGC,TGC | R139C | NP_872586.1 |
XM_005266883.2 | 438 | Missense Mutation | CGC,TGC | R139C | XP_005266940.1 |