ENST00000711048.1:c.1009-497C>G
|
ENSP00000518557.1:n.1009-497C>G
|
|
ENST00000402731.6:c.1029C>G
|
ENSP00000384835.2:p.Cys343Trp
|
|
ENST00000404276.6:c.1230C>G
MANE Select
|
ENSP00000385747.1:p.Cys410Trp
|
|
ENST00000425190.7:c.567C>G
|
ENSP00000390244.2:p.Cys189Trp
|
|
ENST00000464581.6:c.570C>G
|
ENSP00000483777.2:p.Cys190Trp
|
|
ENST00000648295.1:n.782C>G
|
|
|
ENST00000649563.1:c.567C>G
|
ENSP00000496928.1:p.Cys189Trp
|
|
ENST00000650281.1:c.1230C>G
|
ENSP00000497000.1:p.Cys410Trp
|
|
ENST00000328354.10:c.1230C>G
|
ENSP00000329178.6:p.Cys410Trp
|
|
ENST00000348295.7:c.1143C>G
|
ENSP00000329012.5:p.Cys381Trp
|
|
ENST00000382580.6:c.1359C>G
|
ENSP00000372023.2:p.Cys453Trp
|
|
ENST00000402731.5:c.1143C>G
|
ENSP00000384835.1:p.Cys381Trp
|
|
ENST00000403642.5:c.957C>G
|
ENSP00000384919.1:p.Cys319Trp
|
|
ENST00000404276.5:c.1230C>G
|
ENSP00000385747.1:p.Cys410Trp
|
|
ENST00000405598.5:c.1230C>G
|
ENSP00000386087.1:p.Cys410Trp
|
|
ENST00000416671.5:c.*720C>G
|
ENSP00000402225.1:n.*720C>G
|
|
ENST00000417588.5:c.1139C>G
|
ENSP00000412901.1:n.1139C>G
|
|
ENST00000433728.5:c.1168C>G
|
ENSP00000404400.1:n.1168C>G
|
|
ENST00000434810.5:c.461C>G
|
|
|
ENST00000448511.5:c.1120C>G
|
ENSP00000404567.1:n.1120C>G
|
|
ENST00000456369.5:c.263+4099C>G
|
|
|
NM_001005735.1:c.1359C>G
|
NP_001005735.1:p.Cys453Trp
|
|
NM_001257387.1:c.567C>G
|
NP_001244316.1:p.Cys189Trp
|
|
NM_007194.3:c.1230C>G
|
NP_009125.1:p.Cys410Trp
|
|
NM_145862.2:c.1143C>G
|
NP_665861.1:p.Cys381Trp
|
|
XM_006724114.2:c.750C>G
|
XP_006724177.1:p.Cys250Trp
|
|
XM_006724116.2:c.687C>G
|
XP_006724179.2:p.Cys229Trp
|
|
XM_011529839.1:c.1389C>G
|
XP_011528141.1:p.Cys463Trp
|
|
XM_011529840.1:c.1302C>G
|
XP_011528142.1:p.Cys434Trp
|
|
XM_011529841.1:c.1158C>G
|
XP_011528143.1:p.Cys386Trp
|
|
XM_011529842.1:c.1059C>G
|
XP_011528144.1:p.Cys353Trp
|
|
XM_011529843.1:c.1029C>G
|
XP_011528145.1:p.Cys343Trp
|
|
XM_011529845.1:c.567C>G
|
XP_011528147.1:p.Cys189Trp
|
|
XR_937805.1:n.1389C>G
|
|
|
NM_001349956.1:c.1029C>G
|
NP_001336885.1:p.Cys343Trp
|
|
NM_007194.4:c.1230C>G
MANE Select
|
NP_009125.1:p.Cys410Trp
|
|
XM_006724114.3:c.783C>G
|
XP_006724177.2:p.Cys261Trp
|
|
XM_011529839.2:c.1389C>G
|
XP_011528141.1:p.Cys463Trp
|
|
XM_011529840.3:c.1302C>G
|
XP_011528142.1:p.Cys434Trp
|
|
XM_011529842.2:c.1059C>G
|
XP_011528144.1:p.Cys353Trp
|
|
XM_011529845.2:c.567C>G
|
XP_011528147.1:p.Cys189Trp
|
|
XM_017028560.1:c.1353C>G
|
XP_016884049.1:p.Cys451Trp
|
|
XM_017028561.2:c.567C>G
|
XP_016884050.1:p.Cys189Trp
|
|
XM_024452148.1:c.1260C>G
|
XP_024307916.1:p.Cys420Trp
|
|
XM_024452149.1:c.1173C>G
|
XP_024307917.1:p.Cys391Trp
|
|
XR_937805.2:n.1400C>G
|
|
|
NM_001005735.2:c.1359C>G
|
NP_001005735.1:p.Cys453Trp
|
|
NM_001257387.2:c.567C>G
|
NP_001244316.1:p.Cys189Trp
|
|
NM_001349956.2:c.1029C>G
|
NP_001336885.1:p.Cys343Trp
|
|