Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001166538.1 | 532 | Intron | NP_001160010.1 | ||
NM_007161.3 | 532 | Intron | NP_009092.3 | ||
NM_205837.2 | 532 | Intron | NP_995309.2 | ||
NM_205838.2 | 532 | Intron | NP_995310.2 | ||
NM_205839.2 | 532 | Intron | NP_995311.2 | ||
NM_205840.2 | 532 | Intron | NP_995312.2 | ||
XM_006715206.3 | 532 | Intron | XP_006715269.1 | ||
XM_006715209.3 | 532 | Intron | XP_006715272.1 | ||
XM_006715210.3 | 532 | Intron | XP_006715273.1 | ||
XM_011514914.2 | 532 | Intron | XP_011513216.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145466.1 | 532 | Missense Mutation | AGC,TGC | S108C | NP_001138938.1 |
NM_001145467.1 | 532 | Missense Mutation | AGC,TGC | S108C | NP_001138939.1 |
NM_147130.2 | 532 | Missense Mutation | AGC,TGC | S108C | NP_667341.1 |
XM_006715049.3 | 532 | Missense Mutation | AGC,TGC | S108C | XP_006715112.1 |
XM_011514459.2 | 532 | Missense Mutation | AGC,TGC | S83C | XP_011512761.1 |