Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_018463.3 | 432 | Missense Mutation | GCC,TCC | A98S | NP_060933.3 |
XM_005253707.4 | 432 | Missense Mutation | GCC,TCC | A98S | XP_005253764.1 |
XM_005253709.4 | 432 | Intron | XP_005253766.1 | ||
XM_017019641.1 | 432 | Intron | XP_016875130.1 |