Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_004687.4 | 3555 | Missense Mutation | CGC,TGC | R1110C | NP_004678.3 |
XM_005257784.2 | 3555 | Missense Mutation | CGC,TGC | R1124C | XP_005257841.1 |
XM_005257785.4 | 3555 | Missense Mutation | CGC,TGC | R1114C | XP_005257842.1 |
XM_005257786.4 | 3555 | Missense Mutation | CGC,TGC | R1110C | XP_005257843.1 |
XM_006722168.3 | 3555 | Missense Mutation | CGC,TGC | R1110C | XP_006722231.1 |
XM_011525460.2 | 3555 | Missense Mutation | CGC,TGC | R1114C | XP_011523762.1 |