ENST00000356592.8:c.680T>G
|
|
|
ENST00000361925.9:c.838T>G
|
ENSP00000354651.5:p.Phe280Val
|
|
ENST00000522053.2:n.609T>G
|
|
|
ENST00000523372.2:c.801T>G
|
|
|
ENST00000638552.1:c.433T>G
|
ENSP00000491763.1:p.Phe145Val
|
|
ENST00000638660.1:c.433T>G
|
ENSP00000492869.1:p.Phe145Val
|
|
ENST00000638772.1:c.718T>G
|
ENSP00000491557.1:p.Phe240Val
|
|
ENST00000638782.1:n.780T>G
|
|
|
ENST00000638877.1:c.595T>G
|
|
|
ENST00000639046.1:c.109T>G
|
ENSP00000492659.1:p.Phe37Val
|
|
ENST00000639111.2:c.718T>G
|
ENSP00000492125.2:p.Phe240Val
|
|
ENST00000639213.2:c.718T>G
MANE Select
|
ENSP00000491909.2:p.Phe240Val
|
|
ENST00000639278.1:c.646T>G
|
ENSP00000491958.1:p.Phe216Val
|
|
ENST00000639384.1:c.718T>G
|
ENSP00000491240.1:p.Phe240Val
|
|
ENST00000639424.1:c.107+35869T>G
|
ENSP00000491245.1:n.107+35869T>G
|
|
ENST00000639683.1:c.652T>G
|
ENSP00000492581.1:p.Phe218Val
|
|
ENST00000639975.1:c.652T>G
|
ENSP00000492096.1:p.Phe218Val
|
|
ENST00000640574.1:c.433T>G
|
ENSP00000491582.1:p.Phe145Val
|
|
ENST00000640739.1:n.3249T>G
|
|
|
ENST00000640910.1:c.156T>G
|
|
|
ENST00000640985.1:c.631T>G
|
ENSP00000492293.1:p.Phe211Val
|
|
ENST00000641017.1:c.718T>G
|
ENSP00000493461.1:p.Phe240Val
|
|
ENST00000356592.7:c.718T>G
|
ENSP00000349000.3:p.Phe240Val
|
|
ENST00000361925.8:c.718T>G
|
ENSP00000354651.4:p.Phe240Val
|
|
ENST00000414552.6:c.838T>G
|
ENSP00000410732.2:p.Phe280Val
|
|
ENST00000522053.1:c.433T>G
|
ENSP00000430182.1:p.Phe145Val
|
|
ENST00000522990.5:c.*320T>G
|
ENSP00000430732.1:n.*320T>G
|
|
ENST00000523372.1:c.839T>G
|
ENSP00000430124.1:n.839T>G
|
|
NM_000816.3:c.718T>G
|
NP_000807.2:p.Phe240Val
|
|
NM_198903.2:c.838T>G
|
NP_944493.2:p.Phe280Val
|
|
NM_198904.2:c.718T>G
|
NP_944494.1:p.Phe240Val
|
|
NM_001375339.1:c.709T>G
|
NP_001362268.1:p.Phe237Val
|
|
NM_001375340.1:c.718T>G
|
NP_001362269.1:p.Phe240Val
|
|
NM_001375341.1:c.718T>G
|
NP_001362270.1:p.Phe240Val
|
|
NM_001375342.1:c.718T>G
|
NP_001362271.1:p.Phe240Val
|
|
NM_001375343.1:c.838T>G
|
NP_001362272.1:p.Phe280Val
|
|
NM_001375344.1:c.718T>G
|
NP_001362273.1:p.Phe240Val
|
|
NM_001375345.1:c.652T>G
|
NP_001362274.1:p.Phe218Val
|
|
NM_001375346.1:c.652T>G
|
NP_001362275.1:p.Phe218Val
|
|
NM_001375347.1:c.631T>G
|
NP_001362276.1:p.Phe211Val
|
|
NM_001375348.1:c.298T>G
|
NP_001362277.1:p.Phe100Val
|
|
NM_001375349.1:c.433T>G
|
NP_001362278.1:p.Phe145Val
|
|
NM_001375350.1:c.298T>G
|
NP_001362279.1:p.Phe100Val
|
|
NM_198904.3:c.718T>G
|
NP_944494.1:p.Phe240Val
|
|
NM_198904.4:c.718T>G
MANE Select
|
NP_944494.1:p.Phe240Val
|
|