ENST00000356592.8:c.1337A>G
|
|
|
ENST00000361925.9:c.1432A>G
|
ENSP00000354651.5:p.Ile478Val
|
|
ENST00000523372.2:c.1395A>G
|
|
|
ENST00000638253.1:n.590A>G
|
|
|
ENST00000638552.1:c.1027A>G
|
ENSP00000491763.1:p.Ile343Val
|
|
ENST00000638660.1:c.1051A>G
|
ENSP00000492869.1:p.Ile351Val
|
|
ENST00000638772.1:c.*3933A>G
|
ENSP00000491557.1:n.*3933A>G
|
|
ENST00000638877.1:c.1213A>G
|
|
|
ENST00000639046.1:c.703A>G
|
ENSP00000492659.1:p.Ile235Val
|
|
ENST00000639111.2:c.1312A>G
|
ENSP00000492125.2:p.Ile438Val
|
|
ENST00000639213.2:c.1336A>G
MANE Select
|
ENSP00000491909.2:p.Ile446Val
|
|
ENST00000639278.1:c.1999A>G
|
ENSP00000491958.1:n.1999A>G
|
|
ENST00000639384.1:c.*1517A>G
|
ENSP00000491240.1:n.*1517A>G
|
|
ENST00000639424.1:c.*536A>G
|
ENSP00000491245.1:n.*536A>G
|
|
ENST00000639683.1:c.1270A>G
|
ENSP00000492581.1:p.Ile424Val
|
|
ENST00000639975.1:c.1246A>G
|
ENSP00000492096.1:p.Ile416Val
|
|
ENST00000640500.1:n.610A>G
|
|
|
ENST00000640739.1:n.6283A>G
|
|
|
ENST00000640910.1:c.774A>G
|
|
|
ENST00000640985.1:c.1249A>G
|
ENSP00000492293.1:p.Ile417Val
|
|
ENST00000641017.1:c.1405A>G
|
ENSP00000493461.1:p.Ile469Val
|
|
ENST00000356592.7:c.1336A>G
|
ENSP00000349000.3:p.Ile446Val
|
|
ENST00000361925.8:c.1312A>G
|
ENSP00000354651.4:p.Ile438Val
|
|
ENST00000414552.6:c.1456A>G
|
ENSP00000410732.2:p.Ile486Val
|
|
ENST00000522990.5:c.*914A>G
|
ENSP00000430732.1:n.*914A>G
|
|
ENST00000523372.1:c.1433A>G
|
ENSP00000430124.1:n.1433A>G
|
|
NM_000816.3:c.1312A>G
|
NP_000807.2:p.Ile438Val
|
|
NM_198903.2:c.1456A>G
|
NP_944493.2:p.Ile486Val
|
|
NM_198904.2:c.1336A>G
|
NP_944494.1:p.Ile446Val
|
|
NM_001375339.1:c.1327A>G
|
NP_001362268.1:p.Ile443Val
|
|
NM_001375340.1:c.*170A>G
|
NP_001362269.1:n.*170A>G
|
|
NM_001375341.1:c.1333A>G
|
NP_001362270.1:p.Ile445Val
|
|
NM_001375342.1:c.1309A>G
|
NP_001362271.1:p.Ile437Val
|
|
NM_001375343.1:c.1432A>G
|
NP_001362272.1:p.Ile478Val
|
|
NM_001375344.1:c.1375A>G
|
NP_001362273.1:p.Ile459Val
|
|
NM_001375345.1:c.1246A>G
|
NP_001362274.1:p.Ile416Val
|
|
NM_001375346.1:c.1270A>G
|
NP_001362275.1:p.Ile424Val
|
|
NM_001375347.1:c.1249A>G
|
NP_001362276.1:p.Ile417Val
|
|
NM_001375348.1:c.892A>G
|
NP_001362277.1:p.Ile298Val
|
|
NM_001375349.1:c.1027A>G
|
NP_001362278.1:p.Ile343Val
|
|
NM_001375350.1:c.916A>G
|
NP_001362279.1:p.Ile306Val
|
|
NM_198904.3:c.1336A>G
|
NP_944494.1:p.Ile446Val
|
|
NM_198904.4:c.1336A>G
MANE Select
|
NP_944494.1:p.Ile446Val
|
|