|
ENST00000264731.8:c.1682G>A
MANE Select
|
ENSP00000264731.3:p.Cys561Tyr
|
|
|
ENST00000354600.10:c.1400G>A
MANE Plus Clinical
|
ENSP00000346614.5:p.Cys467Tyr
|
|
|
ENST00000264731.7:c.1682G>A
|
ENSP00000264731.3:p.Cys561Tyr
|
|
|
ENST00000320472.9:c.1508-3388G>A
|
ENSP00000317510.5:n.1508-3388G>A
|
|
|
ENST00000354600.9:c.1400G>A
|
ENSP00000346614.5:p.Cys467Tyr
|
|
|
ENST00000392460.7:c.1652+1334G>A
|
ENSP00000376253.3:n.1652+1334G>A
|
|
|
ENST00000392461.7:c.1226-3388G>A
|
ENSP00000376254.3:n.1226-3388G>A
|
|
|
ENST00000392463.6:c.1370+1334G>A
|
ENSP00000376256.2:n.1370+1334G>A
|
|
|
ENST00000440651.6:c.1670G>A
|
ENSP00000394337.2:p.Cys557Tyr
|
|
|
ENST00000449992.5:c.1145G>A
|
ENSP00000387839.1:p.Cys382Tyr
|
|
|
ENST00000456148.1:c.1388G>A
|
ENSP00000389485.1:p.Cys463Tyr
|
|
|
NM_001114978.1:c.1652+1334G>A
|
NP_001108450.1:n.1652+1334G>A
|
|
|
NM_001114980.1:c.1400G>A
|
NP_001108452.1:p.Cys467Tyr
|
|
|
NM_001114981.1:c.1370+1334G>A
|
NP_001108453.1:n.1370+1334G>A
|
|
|
NM_003722.4:c.1682G>A
|
NP_003713.3:p.Cys561Tyr
|
|
|
XM_005247843.2:c.1670G>A
|
XP_005247900.1:p.Cys557Tyr
|
|
|
XM_005247844.3:c.1631G>A
|
XP_005247901.1:p.Cys544Tyr
|
|
|
XM_011513251.1:c.1679G>A
|
XP_011511553.1:p.Cys560Tyr
|
|
|
XM_011513252.1:c.1676G>A
|
XP_011511554.1:p.Cys559Tyr
|
|
|
XM_011513253.1:c.1643G>A
|
XP_011511555.1:p.Cys548Tyr
|
|
|
NM_001329144.1:c.1508-3388G>A
|
NP_001316073.1:n.1508-3388G>A
|
|
|
NM_001329145.1:c.1226-3388G>A
|
NP_001316074.1:n.1226-3388G>A
|
|
|
NM_001329146.1:c.1145G>A
|
NP_001316075.1:p.Cys382Tyr
|
|
|
NM_001329148.1:c.1670G>A
|
NP_001316077.1:p.Cys557Tyr
|
|
|
NM_001329149.1:c.1214-3388G>A
|
NP_001316078.1:n.1214-3388G>A
|
|
|
NM_001329150.1:c.959-3388G>A
|
NP_001316079.1:n.959-3388G>A
|
|
|
NM_001329964.1:c.1676G>A
|
NP_001316893.1:p.Cys559Tyr
|
|
|
NM_003722.5:c.1682G>A
MANE Select
|
NP_003713.3:p.Cys561Tyr
|
|
|
NM_001114978.2:c.1652+1334G>A
|
NP_001108450.1:n.1652+1334G>A
|
|
|
NM_001114980.2:c.1400G>A
MANE Plus Clinical
|
NP_001108452.1:p.Cys467Tyr
|
|
|
NM_001114981.2:c.1370+1334G>A
|
NP_001108453.1:n.1370+1334G>A
|
|
|
NM_001329144.2:c.1508-3388G>A
|
NP_001316073.1:n.1508-3388G>A
|
|
|
NM_001329145.2:c.1226-3388G>A
|
NP_001316074.1:n.1226-3388G>A
|
|
|
NM_001329146.2:c.1145G>A
|
NP_001316075.1:p.Cys382Tyr
|
|
|
NM_001329148.2:c.1670G>A
|
NP_001316077.1:p.Cys557Tyr
|
|
|
NM_001329149.2:c.1214-3388G>A
|
NP_001316078.1:n.1214-3388G>A
|
|
|
NM_001329150.2:c.959-3388G>A
|
NP_001316079.1:n.959-3388G>A
|
|
|
NM_001329964.2:c.1676G>A
|
NP_001316893.1:p.Cys559Tyr
|
|
