ENST00000356592.8:c.1445A>G
|
|
|
ENST00000361925.9:c.*16A>G
|
ENSP00000354651.5:n.*16A>G
|
|
ENST00000523372.2:c.1503A>G
|
|
|
ENST00000638253.1:n.698A>G
|
|
|
ENST00000638552.1:c.*16A>G
|
ENSP00000491763.1:n.*16A>G
|
|
ENST00000638660.1:c.*16A>G
|
ENSP00000492869.1:n.*16A>G
|
|
ENST00000638772.1:c.*4041A>G
|
ENSP00000491557.1:n.*4041A>G
|
|
ENST00000638877.1:c.1321A>G
|
|
|
ENST00000639046.1:c.*16A>G
|
ENSP00000492659.1:n.*16A>G
|
|
ENST00000639111.2:c.*16A>G
|
ENSP00000492125.2:n.*16A>G
|
|
ENST00000639213.2:c.*16A>G
MANE Select
|
ENSP00000491909.2:n.*16A>G
|
|
ENST00000639278.1:c.2107A>G
|
ENSP00000491958.1:n.2107A>G
|
|
ENST00000639384.1:c.*1625A>G
|
ENSP00000491240.1:n.*1625A>G
|
|
ENST00000639424.1:c.*644A>G
|
ENSP00000491245.1:n.*644A>G
|
|
ENST00000639683.1:c.*16A>G
|
ENSP00000492581.1:n.*16A>G
|
|
ENST00000639975.1:c.*16A>G
|
ENSP00000492096.1:n.*16A>G
|
|
ENST00000640500.1:n.718A>G
|
|
|
ENST00000640739.1:n.6391A>G
|
|
|
ENST00000640910.1:c.882A>G
|
|
|
ENST00000640985.1:c.*16A>G
|
ENSP00000492293.1:n.*16A>G
|
|
ENST00000641017.1:c.1513A>G
|
ENSP00000493461.1:n.1513A>G
|
|
ENST00000356592.7:c.*16A>G
|
ENSP00000349000.3:n.*16A>G
|
|
ENST00000361925.8:c.*16A>G
|
ENSP00000354651.4:n.*16A>G
|
|
ENST00000414552.6:c.*16A>G
|
ENSP00000410732.2:n.*16A>G
|
|
ENST00000522990.5:c.*1022A>G
|
ENSP00000430732.1:n.*1022A>G
|
|
ENST00000523372.1:c.1541A>G
|
ENSP00000430124.1:n.1541A>G
|
|
NM_000816.3:c.*16A>G
|
NP_000807.2:n.*16A>G
|
|
NM_198903.2:c.*16A>G
|
NP_944493.2:n.*16A>G
|
|
NM_198904.2:c.*16A>G
|
NP_944494.1:n.*16A>G
|
|
NM_001375339.1:c.*16A>G
|
NP_001362268.1:n.*16A>G
|
|
NM_001375340.1:c.*278A>G
|
NP_001362269.1:n.*278A>G
|
|
NM_001375341.1:c.*16A>G
|
NP_001362270.1:n.*16A>G
|
|
NM_001375342.1:c.*16A>G
|
NP_001362271.1:n.*16A>G
|
|
NM_001375343.1:c.*16A>G
|
NP_001362272.1:n.*16A>G
|
|
NM_001375344.1:c.*16A>G
|
NP_001362273.1:n.*16A>G
|
|
NM_001375345.1:c.*16A>G
|
NP_001362274.1:n.*16A>G
|
|
NM_001375346.1:c.*16A>G
|
NP_001362275.1:n.*16A>G
|
|
NM_001375347.1:c.*16A>G
|
NP_001362276.1:n.*16A>G
|
|
NM_001375348.1:c.*16A>G
|
NP_001362277.1:n.*16A>G
|
|
NM_001375349.1:c.*16A>G
|
NP_001362278.1:n.*16A>G
|
|
NM_001375350.1:c.*16A>G
|
NP_001362279.1:n.*16A>G
|
|
NM_198904.3:c.*16A>G
|
NP_944494.1:n.*16A>G
|
|
NM_198904.4:c.*16A>G
MANE Select
|
NP_944494.1:n.*16A>G
|
|