ENST00000356592.8:c.1373C>G
|
|
|
ENST00000361925.9:c.1468C>G
|
ENSP00000354651.5:p.Pro490Ala
|
|
ENST00000523372.2:c.1431C>G
|
|
|
ENST00000638253.1:n.626C>G
|
|
|
ENST00000638552.1:c.1063C>G
|
ENSP00000491763.1:p.Pro355Ala
|
|
ENST00000638660.1:c.1087C>G
|
ENSP00000492869.1:p.Pro363Ala
|
|
ENST00000638772.1:c.*3969C>G
|
ENSP00000491557.1:n.*3969C>G
|
|
ENST00000638877.1:c.1249C>G
|
|
|
ENST00000639046.1:c.739C>G
|
ENSP00000492659.1:p.Pro247Ala
|
|
ENST00000639111.2:c.1348C>G
|
ENSP00000492125.2:p.Pro450Ala
|
|
ENST00000639213.2:c.1372C>G
MANE Select
|
ENSP00000491909.2:p.Pro458Ala
|
|
ENST00000639278.1:c.2035C>G
|
ENSP00000491958.1:n.2035C>G
|
|
ENST00000639384.1:c.*1553C>G
|
ENSP00000491240.1:n.*1553C>G
|
|
ENST00000639424.1:c.*572C>G
|
ENSP00000491245.1:n.*572C>G
|
|
ENST00000639683.1:c.1306C>G
|
ENSP00000492581.1:p.Pro436Ala
|
|
ENST00000639975.1:c.1282C>G
|
ENSP00000492096.1:p.Pro428Ala
|
|
ENST00000640500.1:n.646C>G
|
|
|
ENST00000640739.1:n.6319C>G
|
|
|
ENST00000640910.1:c.810C>G
|
|
|
ENST00000640985.1:c.1285C>G
|
ENSP00000492293.1:p.Pro429Ala
|
|
ENST00000641017.1:c.1441C>G
|
ENSP00000493461.1:p.Pro481Ala
|
|
ENST00000356592.7:c.1372C>G
|
ENSP00000349000.3:p.Pro458Ala
|
|
ENST00000361925.8:c.1348C>G
|
ENSP00000354651.4:p.Pro450Ala
|
|
ENST00000414552.6:c.1492C>G
|
ENSP00000410732.2:p.Pro498Ala
|
|
ENST00000522990.5:c.*950C>G
|
ENSP00000430732.1:n.*950C>G
|
|
ENST00000523372.1:c.1469C>G
|
ENSP00000430124.1:n.1469C>G
|
|
NM_000816.3:c.1348C>G
|
NP_000807.2:p.Pro450Ala
|
|
NM_198903.2:c.1492C>G
|
NP_944493.2:p.Pro498Ala
|
|
NM_198904.2:c.1372C>G
|
NP_944494.1:p.Pro458Ala
|
|
NM_001375339.1:c.1363C>G
|
NP_001362268.1:p.Pro455Ala
|
|
NM_001375340.1:c.*206C>G
|
NP_001362269.1:n.*206C>G
|
|
NM_001375341.1:c.1369C>G
|
NP_001362270.1:p.Pro457Ala
|
|
NM_001375342.1:c.1345C>G
|
NP_001362271.1:p.Pro449Ala
|
|
NM_001375343.1:c.1468C>G
|
NP_001362272.1:p.Pro490Ala
|
|
NM_001375344.1:c.1411C>G
|
NP_001362273.1:p.Pro471Ala
|
|
NM_001375345.1:c.1282C>G
|
NP_001362274.1:p.Pro428Ala
|
|
NM_001375346.1:c.1306C>G
|
NP_001362275.1:p.Pro436Ala
|
|
NM_001375347.1:c.1285C>G
|
NP_001362276.1:p.Pro429Ala
|
|
NM_001375348.1:c.928C>G
|
NP_001362277.1:p.Pro310Ala
|
|
NM_001375349.1:c.1063C>G
|
NP_001362278.1:p.Pro355Ala
|
|
NM_001375350.1:c.952C>G
|
NP_001362279.1:p.Pro318Ala
|
|
NM_198904.3:c.1372C>G
|
NP_944494.1:p.Pro458Ala
|
|
NM_198904.4:c.1372C>G
MANE Select
|
NP_944494.1:p.Pro458Ala
|
|