ENST00000356592.8:c.1111T=
|
|
|
ENST00000361925.9:c.1230T=
|
ENSP00000354651.5:p.Asp410=
|
|
ENST00000523372.2:c.1193T=
|
|
|
ENST00000638253.1:n.364T=
|
|
|
ENST00000638552.1:c.825T=
|
ENSP00000491763.1:p.Asp275=
|
|
ENST00000638660.1:c.825T=
|
ENSP00000492869.1:p.Asp275=
|
|
ENST00000638772.1:c.1110T=
|
ENSP00000491557.1:p.Asp370=
|
|
ENST00000638877.1:c.987T=
|
|
|
ENST00000639046.1:c.501T=
|
ENSP00000492659.1:p.Asp167=
|
|
ENST00000639111.2:c.1110T=
|
ENSP00000492125.2:p.Asp370=
|
|
ENST00000639213.2:c.1110T=
MANE Select
|
ENSP00000491909.2:p.Asp370=
|
|
ENST00000639278.1:c.1038T=
|
ENSP00000491958.1:p.Asp346=
|
|
ENST00000639384.1:c.1110T=
|
ENSP00000491240.1:p.Asp370=
|
|
ENST00000639424.1:c.*310T=
|
ENSP00000491245.1:n.*310T=
|
|
ENST00000639683.1:c.1044T=
|
ENSP00000492581.1:p.Asp348=
|
|
ENST00000639975.1:c.1044T=
|
ENSP00000492096.1:p.Asp348=
|
|
ENST00000640500.1:n.408T=
|
|
|
ENST00000640574.1:c.825T=
|
ENSP00000491582.1:p.Asp275=
|
|
ENST00000640739.1:n.3641T=
|
|
|
ENST00000640910.1:c.548T=
|
|
|
ENST00000640985.1:c.1023T=
|
ENSP00000492293.1:p.Asp341=
|
|
ENST00000641017.1:c.1110T=
|
ENSP00000493461.1:p.Asp370=
|
|
ENST00000356592.7:c.1110T=
|
ENSP00000349000.3:p.Asp370=
|
|
ENST00000361925.8:c.1110T=
|
ENSP00000354651.4:p.Asp370=
|
|
ENST00000414552.6:c.1230T=
|
ENSP00000410732.2:p.Asp410=
|
|
ENST00000522990.5:c.*712T=
|
ENSP00000430732.1:n.*712T=
|
|
ENST00000523372.1:c.1231T=
|
ENSP00000430124.1:n.1231T=
|
|
NM_000816.3:c.1110T=
|
NP_000807.2:p.Asp370=
|
|
NM_198903.2:c.1230T=
|
NP_944493.2:p.Asp410=
|
|
NM_198904.2:c.1110T=
|
NP_944494.1:p.Asp370=
|
|
NM_001375339.1:c.1101T=
|
NP_001362268.1:p.Asp367=
|
|
NM_001375340.1:c.923-2435T=
|
NP_001362269.1:n.923-2435T=
|
|
NM_001375341.1:c.1107T=
|
NP_001362270.1:p.Asp369=
|
|
NM_001375342.1:c.1107T=
|
NP_001362271.1:p.Asp369=
|
|
NM_001375343.1:c.1230T=
|
NP_001362272.1:p.Asp410=
|
|
NM_001375344.1:c.1149T=
|
NP_001362273.1:p.Asp383=
|
|
NM_001375345.1:c.1044T=
|
NP_001362274.1:p.Asp348=
|
|
NM_001375346.1:c.1044T=
|
NP_001362275.1:p.Asp348=
|
|
NM_001375347.1:c.1023T=
|
NP_001362276.1:p.Asp341=
|
|
NM_001375348.1:c.690T=
|
NP_001362277.1:p.Asp230=
|
|
NM_001375349.1:c.825T=
|
NP_001362278.1:p.Asp275=
|
|
NM_001375350.1:c.690T=
|
NP_001362279.1:p.Asp230=
|
|
NM_198904.3:c.1110T=
|
NP_944494.1:p.Asp370=
|
|
NM_198904.4:c.1110T=
MANE Select
|
NP_944494.1:p.Asp370=
|
|