ENST00000682424.1:c.1125_1126insTTCAGT
|
ENSP00000507321.1:p.Ser375_Asn376insPheSer
|
|
ENST00000299427.12:c.1239_1240insTTCAGT
MANE Select
|
ENSP00000299427.6:p.Ser413_Asn414insPheSer
|
|
ENST00000436873.7:c.476_477insTTCAGT
|
|
|
ENST00000524924.2:n.359_360insTTCAGT
|
|
|
ENST00000533371.6:c.510_511insTTCAGT
|
ENSP00000437066.1:p.Ser170_Asn171insPheSer
|
|
ENST00000642892.1:c.510_511insTTCAGT
|
ENSP00000494165.1:p.Ser170_Asn171insPheSer
|
|
ENST00000643342.1:c.312_313insTTCAGT
|
|
|
ENST00000643439.1:c.*979_*980insTTCAGT
|
ENSP00000495849.1:n.*979_*980insTTCAGT
|
|
ENST00000643479.1:n.1425_1426insTTCAGT
|
|
|
ENST00000643516.1:c.748_749insTTCAGT
|
|
|
ENST00000644218.1:c.1050_1051insTTCAGT
|
ENSP00000493574.1:p.Ser350_Asn351insPheSer
|
|
ENST00000644683.1:c.*692_*693insTTCAGT
|
ENSP00000494085.1:n.*692_*693insTTCAGT
|
|
ENST00000644810.1:c.960_961insTTCAGT
|
ENSP00000495895.1:p.Ser320_Asn321insPheSer
|
|
ENST00000644831.1:n.1415_1416insTTCAGT
|
|
|
ENST00000644933.1:c.*105_*106insTTCAGT
|
ENSP00000496133.1:n.*105_*106insTTCAGT
|
|
ENST00000645285.1:c.*105_*106insTTCAGT
|
ENSP00000495058.1:n.*105_*106insTTCAGT
|
|
ENST00000645331.1:n.2444_2445insTTCAGT
|
|
|
ENST00000645620.1:c.510_511insTTCAGT
|
ENSP00000493657.1:p.Ser170_Asn171insPheSer
|
|
ENST00000646691.1:n.1014_1015insTTCAGT
|
|
|
ENST00000646777.1:n.1572_1573insTTCAGT
|
|
|
ENST00000647016.1:n.1719_1720insTTCAGT
|
|
|
ENST00000647152.1:c.510_511insTTCAGT
|
ENSP00000495893.1:p.Ser170_Asn171insPheSer
|
|
ENST00000647209.1:c.*1108_*1109insTTCAGT
|
ENSP00000495558.1:n.*1108_*1109insTTCAGT
|
|
ENST00000647346.1:n.2259_2260insTTCAGT
|
|
|
ENST00000299427.10:c.1239_1240insTTCAGT
|
ENSP00000299427.6:p.Ser413_Asn414insPheSer
|
|
ENST00000524611.1:n.5_6insTTCAGT
|
|
|
ENST00000524924.1:n.194_195insTTCAGT
|
|
|
ENST00000532191.1:n.292_293insTTCAGT
|
|
|
ENST00000533371.5:c.510_511insTTCAGT
|
ENSP00000437066.1:p.Ser170_Asn171insPheSer
|
|
ENST00000611494.4:c.1239_1240insTTCAGT
|
ENSP00000484546.1:p.Ser413_Asn414insPheSer
|
|
NM_000391.3:c.1239_1240insTTCAGT
|
NP_000382.3:p.Ser413_Asn414insPheSer
|
|
NM_000391.4:c.1239_1240insTTCAGT
MANE Select
|
NP_000382.3:p.Ser413_Asn414insPheSer
|
|