ENST00000356592.8:c.1337A>T
|
|
|
ENST00000361925.9:c.1432A>T
|
ENSP00000354651.5:p.Ile478Phe
|
|
ENST00000523372.2:c.1395A>T
|
|
|
ENST00000638253.1:n.590A>T
|
|
|
ENST00000638552.1:c.1027A>T
|
ENSP00000491763.1:p.Ile343Phe
|
|
ENST00000638660.1:c.1051A>T
|
ENSP00000492869.1:p.Ile351Phe
|
|
ENST00000638772.1:c.*3933A>T
|
ENSP00000491557.1:n.*3933A>T
|
|
ENST00000638877.1:c.1213A>T
|
|
|
ENST00000639046.1:c.703A>T
|
ENSP00000492659.1:p.Ile235Phe
|
|
ENST00000639111.2:c.1312A>T
|
ENSP00000492125.2:p.Ile438Phe
|
|
ENST00000639213.2:c.1336A>T
MANE Select
|
ENSP00000491909.2:p.Ile446Phe
|
|
ENST00000639278.1:c.1999A>T
|
ENSP00000491958.1:n.1999A>T
|
|
ENST00000639384.1:c.*1517A>T
|
ENSP00000491240.1:n.*1517A>T
|
|
ENST00000639424.1:c.*536A>T
|
ENSP00000491245.1:n.*536A>T
|
|
ENST00000639683.1:c.1270A>T
|
ENSP00000492581.1:p.Ile424Phe
|
|
ENST00000639975.1:c.1246A>T
|
ENSP00000492096.1:p.Ile416Phe
|
|
ENST00000640500.1:n.610A>T
|
|
|
ENST00000640739.1:n.6283A>T
|
|
|
ENST00000640910.1:c.774A>T
|
|
|
ENST00000640985.1:c.1249A>T
|
ENSP00000492293.1:p.Ile417Phe
|
|
ENST00000641017.1:c.1405A>T
|
ENSP00000493461.1:p.Ile469Phe
|
|
ENST00000356592.7:c.1336A>T
|
ENSP00000349000.3:p.Ile446Phe
|
|
ENST00000361925.8:c.1312A>T
|
ENSP00000354651.4:p.Ile438Phe
|
|
ENST00000414552.6:c.1456A>T
|
ENSP00000410732.2:p.Ile486Phe
|
|
ENST00000522990.5:c.*914A>T
|
ENSP00000430732.1:n.*914A>T
|
|
ENST00000523372.1:c.1433A>T
|
ENSP00000430124.1:n.1433A>T
|
|
NM_000816.3:c.1312A>T
|
NP_000807.2:p.Ile438Phe
|
|
NM_198903.2:c.1456A>T
|
NP_944493.2:p.Ile486Phe
|
|
NM_198904.2:c.1336A>T
|
NP_944494.1:p.Ile446Phe
|
|
NM_001375339.1:c.1327A>T
|
NP_001362268.1:p.Ile443Phe
|
|
NM_001375340.1:c.*170A>T
|
NP_001362269.1:n.*170A>T
|
|
NM_001375341.1:c.1333A>T
|
NP_001362270.1:p.Ile445Phe
|
|
NM_001375342.1:c.1309A>T
|
NP_001362271.1:p.Ile437Phe
|
|
NM_001375343.1:c.1432A>T
|
NP_001362272.1:p.Ile478Phe
|
|
NM_001375344.1:c.1375A>T
|
NP_001362273.1:p.Ile459Phe
|
|
NM_001375345.1:c.1246A>T
|
NP_001362274.1:p.Ile416Phe
|
|
NM_001375346.1:c.1270A>T
|
NP_001362275.1:p.Ile424Phe
|
|
NM_001375347.1:c.1249A>T
|
NP_001362276.1:p.Ile417Phe
|
|
NM_001375348.1:c.892A>T
|
NP_001362277.1:p.Ile298Phe
|
|
NM_001375349.1:c.1027A>T
|
NP_001362278.1:p.Ile343Phe
|
|
NM_001375350.1:c.916A>T
|
NP_001362279.1:p.Ile306Phe
|
|
NM_198904.3:c.1336A>T
|
NP_944494.1:p.Ile446Phe
|
|
NM_198904.4:c.1336A>T
MANE Select
|
NP_944494.1:p.Ile446Phe
|
|