ENST00000356592.8:c.1320G>T
|
|
|
ENST00000361925.9:c.1415G>T
|
ENSP00000354651.5:p.Gly472Val
|
|
ENST00000523372.2:c.1378G>T
|
|
|
ENST00000638253.1:n.573G>T
|
|
|
ENST00000638552.1:c.1010G>T
|
ENSP00000491763.1:p.Gly337Val
|
|
ENST00000638660.1:c.1034G>T
|
ENSP00000492869.1:p.Gly345Val
|
|
ENST00000638772.1:c.*3916G>T
|
ENSP00000491557.1:n.*3916G>T
|
|
ENST00000638877.1:c.1196G>T
|
|
|
ENST00000639046.1:c.686G>T
|
ENSP00000492659.1:p.Gly229Val
|
|
ENST00000639111.2:c.1295G>T
|
ENSP00000492125.2:p.Gly432Val
|
|
ENST00000639213.2:c.1319G>T
MANE Select
|
ENSP00000491909.2:p.Gly440Val
|
|
ENST00000639278.1:c.1982G>T
|
ENSP00000491958.1:n.1982G>T
|
|
ENST00000639384.1:c.*1500G>T
|
ENSP00000491240.1:n.*1500G>T
|
|
ENST00000639424.1:c.*519G>T
|
ENSP00000491245.1:n.*519G>T
|
|
ENST00000639683.1:c.1253G>T
|
ENSP00000492581.1:p.Gly418Val
|
|
ENST00000639975.1:c.1229G>T
|
ENSP00000492096.1:p.Gly410Val
|
|
ENST00000640500.1:n.593G>T
|
|
|
ENST00000640739.1:n.6266G>T
|
|
|
ENST00000640910.1:c.757G>T
|
|
|
ENST00000640985.1:c.1232G>T
|
ENSP00000492293.1:p.Gly411Val
|
|
ENST00000641017.1:c.1388G>T
|
ENSP00000493461.1:p.Gly463Val
|
|
ENST00000356592.7:c.1319G>T
|
ENSP00000349000.3:p.Gly440Val
|
|
ENST00000361925.8:c.1295G>T
|
ENSP00000354651.4:p.Gly432Val
|
|
ENST00000414552.6:c.1439G>T
|
ENSP00000410732.2:p.Gly480Val
|
|
ENST00000522990.5:c.*897G>T
|
ENSP00000430732.1:n.*897G>T
|
|
ENST00000523372.1:c.1416G>T
|
ENSP00000430124.1:n.1416G>T
|
|
NM_000816.3:c.1295G>T
|
NP_000807.2:p.Gly432Val
|
|
NM_198903.2:c.1439G>T
|
NP_944493.2:p.Gly480Val
|
|
NM_198904.2:c.1319G>T
|
NP_944494.1:p.Gly440Val
|
|
NM_001375339.1:c.1310G>T
|
NP_001362268.1:p.Gly437Val
|
|
NM_001375340.1:c.*153G>T
|
NP_001362269.1:n.*153G>T
|
|
NM_001375341.1:c.1316G>T
|
NP_001362270.1:p.Gly439Val
|
|
NM_001375342.1:c.1292G>T
|
NP_001362271.1:p.Gly431Val
|
|
NM_001375343.1:c.1415G>T
|
NP_001362272.1:p.Gly472Val
|
|
NM_001375344.1:c.1358G>T
|
NP_001362273.1:p.Gly453Val
|
|
NM_001375345.1:c.1229G>T
|
NP_001362274.1:p.Gly410Val
|
|
NM_001375346.1:c.1253G>T
|
NP_001362275.1:p.Gly418Val
|
|
NM_001375347.1:c.1232G>T
|
NP_001362276.1:p.Gly411Val
|
|
NM_001375348.1:c.875G>T
|
NP_001362277.1:p.Gly292Val
|
|
NM_001375349.1:c.1010G>T
|
NP_001362278.1:p.Gly337Val
|
|
NM_001375350.1:c.899G>T
|
NP_001362279.1:p.Gly300Val
|
|
NM_198904.3:c.1319G>T
|
NP_944494.1:p.Gly440Val
|
|
NM_198904.4:c.1319G>T
MANE Select
|
NP_944494.1:p.Gly440Val
|
|