ENST00000356592.8:c.1420C>A
|
|
|
ENST00000361925.9:c.1515C>A
|
ENSP00000354651.5:p.Leu505=
|
|
ENST00000523372.2:c.1478C>A
|
|
|
ENST00000638253.1:n.673C>A
|
|
|
ENST00000638552.1:c.1110C>A
|
ENSP00000491763.1:p.Leu370=
|
|
ENST00000638660.1:c.1134C>A
|
ENSP00000492869.1:p.Leu378=
|
|
ENST00000638772.1:c.*4016C>A
|
ENSP00000491557.1:n.*4016C>A
|
|
ENST00000638877.1:c.1296C>A
|
|
|
ENST00000639046.1:c.786C>A
|
ENSP00000492659.1:p.Leu262=
|
|
ENST00000639111.2:c.1395C>A
|
ENSP00000492125.2:p.Leu465=
|
|
ENST00000639213.2:c.1419C>A
MANE Select
|
ENSP00000491909.2:p.Leu473=
|
|
ENST00000639278.1:c.2082C>A
|
ENSP00000491958.1:n.2082C>A
|
|
ENST00000639384.1:c.*1600C>A
|
ENSP00000491240.1:n.*1600C>A
|
|
ENST00000639424.1:c.*619C>A
|
ENSP00000491245.1:n.*619C>A
|
|
ENST00000639683.1:c.1353C>A
|
ENSP00000492581.1:p.Leu451=
|
|
ENST00000639975.1:c.1329C>A
|
ENSP00000492096.1:p.Leu443=
|
|
ENST00000640500.1:n.693C>A
|
|
|
ENST00000640739.1:n.6366C>A
|
|
|
ENST00000640910.1:c.857C>A
|
|
|
ENST00000640985.1:c.1332C>A
|
ENSP00000492293.1:p.Leu444=
|
|
ENST00000641017.1:c.1488C>A
|
ENSP00000493461.1:p.Leu496=
|
|
ENST00000356592.7:c.1419C>A
|
ENSP00000349000.3:p.Leu473=
|
|
ENST00000361925.8:c.1395C>A
|
ENSP00000354651.4:p.Leu465=
|
|
ENST00000414552.6:c.1539C>A
|
ENSP00000410732.2:p.Leu513=
|
|
ENST00000522990.5:c.*997C>A
|
ENSP00000430732.1:n.*997C>A
|
|
ENST00000523372.1:c.1516C>A
|
ENSP00000430124.1:n.1516C>A
|
|
NM_000816.3:c.1395C>A
|
NP_000807.2:p.Leu465=
|
|
NM_198903.2:c.1539C>A
|
NP_944493.2:p.Leu513=
|
|
NM_198904.2:c.1419C>A
|
NP_944494.1:p.Leu473=
|
|
NM_001375339.1:c.1410C>A
|
NP_001362268.1:p.Leu470=
|
|
NM_001375340.1:c.*253C>A
|
NP_001362269.1:n.*253C>A
|
|
NM_001375341.1:c.1416C>A
|
NP_001362270.1:p.Leu472=
|
|
NM_001375342.1:c.1392C>A
|
NP_001362271.1:p.Leu464=
|
|
NM_001375343.1:c.1515C>A
|
NP_001362272.1:p.Leu505=
|
|
NM_001375344.1:c.1458C>A
|
NP_001362273.1:p.Leu486=
|
|
NM_001375345.1:c.1329C>A
|
NP_001362274.1:p.Leu443=
|
|
NM_001375346.1:c.1353C>A
|
NP_001362275.1:p.Leu451=
|
|
NM_001375347.1:c.1332C>A
|
NP_001362276.1:p.Leu444=
|
|
NM_001375348.1:c.975C>A
|
NP_001362277.1:p.Leu325=
|
|
NM_001375349.1:c.1110C>A
|
NP_001362278.1:p.Leu370=
|
|
NM_001375350.1:c.999C>A
|
NP_001362279.1:p.Leu333=
|
|
NM_198904.3:c.1419C>A
|
NP_944494.1:p.Leu473=
|
|
NM_198904.4:c.1419C>A
MANE Select
|
NP_944494.1:p.Leu473=
|
|