Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001172656.1 | 3217 | Missense Mutation | ATC,CTC | I815L | NP_001166127.1 |
NM_001172657.1 | 3217 | Intron | NP_001166128.1 | ||
NM_001172658.1 | 3217 | Intron | NP_001166129.1 | ||
NM_001172659.1 | 3217 | Missense Mutation | ATC,CTC | I775L | NP_001166130.1 |
NM_001172660.1 | 3217 | Intron | NP_001166131.1 | ||
NM_020972.2 | 3217 | Missense Mutation | ATC,CTC | I845L | NP_066023.2 |
XM_006713900.3 | 3217 | Missense Mutation | GAT,GCT | D948A | XP_006713963.1 |
XM_006713902.3 | 3217 | UTR 3 | XP_006713965.1 | ||
XM_006713904.3 | 3217 | Intron | XP_006713967.1 | ||
XM_011513540.2 | 3217 | Missense Mutation | GAT,GCT | D834A | XP_011511842.1 |
XM_011513541.2 | 3217 | Intron | XP_011511843.1 | ||
XM_017008502.1 | 3217 | Missense Mutation | GAT,GCT | D890A | XP_016863991.1 |
XM_017008503.1 | 3217 | UTR 3 | XP_016863992.1 | ||
XM_017008504.1 | 3217 | Missense Mutation | AGA,AGC | R919S | XP_016863993.1 |
XM_017008505.1 | 3217 | Missense Mutation | ATC,CTC | I731L | XP_016863994.1 |
XM_017008506.1 | 3217 | Intron | XP_016863995.1 | ||
XM_017008507.1 | 3217 | Intron | XP_016863996.1 | ||
XM_017008508.1 | 3217 | Intron | XP_016863997.1 | ||
XM_017008509.1 | 3217 | Intron | XP_016863998.1 | ||
XM_017008510.1 | 3217 | Intron | XP_016863999.1 |