ENST00000356592.8:c.1423C>T
|
|
|
ENST00000361925.9:c.1518C>T
|
ENSP00000354651.5:p.Tyr506=
|
|
ENST00000523372.2:c.1481C>T
|
|
|
ENST00000638253.1:n.676C>T
|
|
|
ENST00000638552.1:c.1113C>T
|
ENSP00000491763.1:p.Tyr371=
|
|
ENST00000638660.1:c.1137C>T
|
ENSP00000492869.1:p.Tyr379=
|
|
ENST00000638772.1:c.*4019C>T
|
ENSP00000491557.1:n.*4019C>T
|
|
ENST00000638877.1:c.1299C>T
|
|
|
ENST00000639046.1:c.789C>T
|
ENSP00000492659.1:p.Tyr263=
|
|
ENST00000639111.2:c.1398C>T
|
ENSP00000492125.2:p.Tyr466=
|
|
ENST00000639213.2:c.1422C>T
MANE Select
|
ENSP00000491909.2:p.Tyr474=
|
|
ENST00000639278.1:c.2085C>T
|
ENSP00000491958.1:n.2085C>T
|
|
ENST00000639384.1:c.*1603C>T
|
ENSP00000491240.1:n.*1603C>T
|
|
ENST00000639424.1:c.*622C>T
|
ENSP00000491245.1:n.*622C>T
|
|
ENST00000639683.1:c.1356C>T
|
ENSP00000492581.1:p.Tyr452=
|
|
ENST00000639975.1:c.1332C>T
|
ENSP00000492096.1:p.Tyr444=
|
|
ENST00000640500.1:n.696C>T
|
|
|
ENST00000640739.1:n.6369C>T
|
|
|
ENST00000640910.1:c.860C>T
|
|
|
ENST00000640985.1:c.1335C>T
|
ENSP00000492293.1:p.Tyr445=
|
|
ENST00000641017.1:c.1491C>T
|
ENSP00000493461.1:p.Tyr497=
|
|
ENST00000356592.7:c.1422C>T
|
ENSP00000349000.3:p.Tyr474=
|
|
ENST00000361925.8:c.1398C>T
|
ENSP00000354651.4:p.Tyr466=
|
|
ENST00000414552.6:c.1542C>T
|
ENSP00000410732.2:p.Tyr514=
|
|
ENST00000522990.5:c.*1000C>T
|
ENSP00000430732.1:n.*1000C>T
|
|
ENST00000523372.1:c.1519C>T
|
ENSP00000430124.1:n.1519C>T
|
|
NM_000816.3:c.1398C>T
|
NP_000807.2:p.Tyr466=
|
|
NM_198903.2:c.1542C>T
|
NP_944493.2:p.Tyr514=
|
|
NM_198904.2:c.1422C>T
|
NP_944494.1:p.Tyr474=
|
|
NM_001375339.1:c.1413C>T
|
NP_001362268.1:p.Tyr471=
|
|
NM_001375340.1:c.*256C>T
|
NP_001362269.1:n.*256C>T
|
|
NM_001375341.1:c.1419C>T
|
NP_001362270.1:p.Tyr473=
|
|
NM_001375342.1:c.1395C>T
|
NP_001362271.1:p.Tyr465=
|
|
NM_001375343.1:c.1518C>T
|
NP_001362272.1:p.Tyr506=
|
|
NM_001375344.1:c.1461C>T
|
NP_001362273.1:p.Tyr487=
|
|
NM_001375345.1:c.1332C>T
|
NP_001362274.1:p.Tyr444=
|
|
NM_001375346.1:c.1356C>T
|
NP_001362275.1:p.Tyr452=
|
|
NM_001375347.1:c.1335C>T
|
NP_001362276.1:p.Tyr445=
|
|
NM_001375348.1:c.978C>T
|
NP_001362277.1:p.Tyr326=
|
|
NM_001375349.1:c.1113C>T
|
NP_001362278.1:p.Tyr371=
|
|
NM_001375350.1:c.1002C>T
|
NP_001362279.1:p.Tyr334=
|
|
NM_198904.3:c.1422C>T
|
NP_944494.1:p.Tyr474=
|
|
NM_198904.4:c.1422C>T
MANE Select
|
NP_944494.1:p.Tyr474=
|
|