Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001167911.1 | 2502 | Missense Mutation | AAC,AGC | N770S | NP_001161383.1 |
NM_001167912.1 | 2502 | Missense Mutation | AAC,AGC | N815S | NP_001161384.1 |
NM_001167915.1 | 2502 | Intron | NP_001161387.1 | ||
NM_001167916.1 | 2502 | Intron | NP_001161388.1 | ||
NM_001167917.1 | 2502 | Intron | NP_001161389.1 | ||
NM_024621.2 | 2502 | Missense Mutation | AAC,AGC | N815S | NP_078897.2 |
XM_011513134.2 | 2502 | Missense Mutation | AAC,AGC | N826S | XP_011511436.1 |
XM_011513135.1 | 2502 | Missense Mutation | AAC,AGC | N770S | XP_011511437.1 |