ENST00000684910.1:c.*654A>G
|
ENSP00000509844.1:n.*654A>G
|
|
ENST00000685439.1:c.776A>G
|
ENSP00000508454.1:p.His259Arg
|
|
ENST00000685944.1:c.1121A>G
|
ENSP00000509266.1:p.His374Arg
|
|
ENST00000686212.1:n.723A>G
|
|
|
ENST00000687215.1:c.*876A>G
|
ENSP00000509706.1:n.*876A>G
|
|
ENST00000688152.1:c.*565A>G
|
ENSP00000509360.1:n.*565A>G
|
|
ENST00000688403.1:c.377A>G
|
ENSP00000508944.1:p.His126Arg
|
|
ENST00000689314.1:c.1166A>G
|
ENSP00000510607.1:p.His389Arg
|
|
ENST00000689694.1:c.1121A>G
|
ENSP00000508718.1:p.His374Arg
|
|
ENST00000689810.1:c.*770A>G
|
ENSP00000510635.1:n.*770A>G
|
|
ENST00000690282.1:c.377A>G
|
ENSP00000509809.1:p.His126Arg
|
|
ENST00000690351.1:c.*773A>G
|
ENSP00000509728.1:n.*773A>G
|
|
ENST00000691232.1:c.776A>G
|
ENSP00000509675.1:p.His259Arg
|
|
ENST00000691482.1:n.2136A>G
|
|
|
ENST00000691686.1:c.1121A>G
|
ENSP00000509784.1:p.His374Arg
|
|
ENST00000691851.1:c.1053+7987A>G
|
ENSP00000510106.1:n.1053+7987A>G
|
|
ENST00000692015.1:c.908A>G
|
ENSP00000510634.1:p.His303Arg
|
|
ENST00000692638.1:c.*926A>G
|
ENSP00000509412.1:n.*926A>G
|
|
ENST00000692852.1:c.932A>G
|
ENSP00000510337.1:p.His311Arg
|
|
ENST00000692915.1:c.*1267A>G
|
ENSP00000508547.1:n.*1267A>G
|
|
ENST00000370396.7:c.1121A>G
MANE Select
|
ENSP00000359423.3:p.His374Arg
|
|
ENST00000306167.11:n.988A>G
|
|
|
ENST00000370396.6:c.1121A>G
|
ENSP00000359423.2:p.His374Arg
|
|
NM_000252.2:c.1121A>G , LRG_839t1:c.1121A>G
|
NP_000243.1:p.His374Arg
|
|
XM_005274687.2:c.1121A>G
|
XP_005274744.1:p.His374Arg
|
|
XM_011531170.1:c.1187A>G
|
XP_011529472.1:p.His396Arg
|
|
XM_011531171.1:c.1166A>G
|
XP_011529473.1:p.His389Arg
|
|
XM_011531172.1:c.1166A>G
|
XP_011529474.1:p.His389Arg
|
|
XM_011531173.1:c.1121A>G
|
XP_011529475.1:p.His374Arg
|
|
XM_011531173.2:c.1121A>G
|
XP_011529475.1:p.His374Arg
|
|
XM_017029547.1:c.1166A>G
|
XP_016885036.1:p.His389Arg
|
|
XM_017029548.1:c.1166A>G
|
XP_016885037.1:p.His389Arg
|
|
XM_017029549.1:c.1121A>G
|
XP_016885038.1:p.His374Arg
|
|
XM_017029550.1:c.1010A>G
|
XP_016885039.1:p.His337Arg
|
|
XM_017029551.2:c.377A>G
|
XP_016885040.1:p.His126Arg
|
|
NM_000252.3:c.1121A>G
MANE Select
|
NP_000243.1:p.His374Arg
|
|
NM_001376906.1:c.1121A>G
|
NP_001363835.1:p.His374Arg
|
|
NM_001376907.1:c.1010A>G
|
NP_001363836.1:p.His337Arg
|
|
NM_001376908.1:c.1121A>G
|
NP_001363837.1:p.His374Arg
|
|