|
ENST00000711048.1:c.*159T>G
|
ENSP00000518557.1:n.*159T>G
|
|
|
ENST00000402731.6:c.1223T>G
|
ENSP00000384835.2:p.Phe408Cys
|
|
|
ENST00000404276.6:c.1424T>G
MANE Select
|
ENSP00000385747.1:p.Phe475Cys
|
|
|
ENST00000425190.7:c.761T>G
|
ENSP00000390244.2:p.Phe254Cys
|
|
|
ENST00000464581.6:c.764T>G
|
ENSP00000483777.2:p.Phe255Cys
|
|
|
ENST00000648295.1:n.976T>G
|
|
|
|
ENST00000649563.1:c.761T>G
|
ENSP00000496928.1:p.Phe254Cys
|
|
|
ENST00000650281.1:c.1424T>G
|
ENSP00000497000.1:p.Phe475Cys
|
|
|
ENST00000328354.10:c.1424T>G
|
ENSP00000329178.6:p.Phe475Cys
|
|
|
ENST00000348295.7:c.1337T>G
|
ENSP00000329012.5:p.Phe446Cys
|
|
|
ENST00000382580.6:c.1553T>G
|
ENSP00000372023.2:p.Phe518Cys
|
|
|
ENST00000402731.5:c.1337T>G
|
ENSP00000384835.1:p.Phe446Cys
|
|
|
ENST00000403642.5:c.1151T>G
|
ENSP00000384919.1:p.Phe384Cys
|
|
|
ENST00000404276.5:c.1424T>G
|
ENSP00000385747.1:p.Phe475Cys
|
|
|
ENST00000405598.5:c.1424T>G
|
ENSP00000386087.1:p.Phe475Cys
|
|
|
ENST00000416671.5:c.*914T>G
|
ENSP00000402225.1:n.*914T>G
|
|
|
ENST00000417588.5:c.1333T>G
|
ENSP00000412901.1:n.1333T>G
|
|
|
ENST00000433728.5:c.1362T>G
|
ENSP00000404400.1:n.1362T>G
|
|
|
ENST00000434810.5:c.622T>G
|
|
|
|
ENST00000448511.5:c.1314T>G
|
ENSP00000404567.1:n.1314T>G
|
|
|
ENST00000456369.5:c.264-4854T>G
|
|
|
|
NM_001005735.1:c.1553T>G
|
NP_001005735.1:p.Phe518Cys
|
|
|
NM_001257387.1:c.761T>G
|
NP_001244316.1:p.Phe254Cys
|
|
|
NM_007194.3:c.1424T>G
|
NP_009125.1:p.Phe475Cys
|
|
|
NM_145862.2:c.1337T>G
|
NP_665861.1:p.Phe446Cys
|
|
|
XM_006724114.2:c.944T>G
|
XP_006724177.1:p.Phe315Cys
|
|
|
XM_006724116.2:c.881T>G
|
XP_006724179.2:p.Phe294Cys
|
|
|
XM_011529839.1:c.1583T>G
|
XP_011528141.1:p.Phe528Cys
|
|
|
XM_011529840.1:c.1496T>G
|
XP_011528142.1:p.Phe499Cys
|
|
|
XM_011529841.1:c.1352T>G
|
XP_011528143.1:p.Phe451Cys
|
|
|
XM_011529842.1:c.1253T>G
|
XP_011528144.1:p.Phe418Cys
|
|
|
XM_011529843.1:c.1223T>G
|
XP_011528145.1:p.Phe408Cys
|
|
|
XM_011529845.1:c.761T>G
|
XP_011528147.1:p.Phe254Cys
|
|
|
XR_937805.1:n.1583T>G
|
|
|
|
NM_001349956.1:c.1223T>G
|
NP_001336885.1:p.Phe408Cys
|
|
|
NM_007194.4:c.1424T>G
MANE Select
|
NP_009125.1:p.Phe475Cys
|
|
|
XM_006724114.3:c.977T>G
|
XP_006724177.2:p.Phe326Cys
|
|
|
XM_011529839.2:c.1583T>G
|
XP_011528141.1:p.Phe528Cys
|
|
|
XM_011529840.3:c.1496T>G
|
XP_011528142.1:p.Phe499Cys
|
|
|
XM_011529842.2:c.1253T>G
|
XP_011528144.1:p.Phe418Cys
|
|
|
XM_011529845.2:c.761T>G
|
XP_011528147.1:p.Phe254Cys
|
|
|
XM_017028560.1:c.1547T>G
|
XP_016884049.1:p.Phe516Cys
|
|
|
XM_017028561.2:c.761T>G
|
XP_016884050.1:p.Phe254Cys
|
|
|
XM_024452148.1:c.1454T>G
|
XP_024307916.1:p.Phe485Cys
|
|
|
XM_024452149.1:c.1367T>G
|
XP_024307917.1:p.Phe456Cys
|
|
|
XR_937805.2:n.1594T>G
|
|
|
|
NM_001005735.2:c.1553T>G
|
NP_001005735.1:p.Phe518Cys
|
|
|
NM_001257387.2:c.761T>G
|
NP_001244316.1:p.Phe254Cys
|
|
|
NM_001349956.2:c.1223T>G
|
NP_001336885.1:p.Phe408Cys
|
|
