ENST00000356592.8:c.731G>T
|
|
|
ENST00000361925.9:c.889G>T
|
ENSP00000354651.5:p.Gly297Ter
|
|
ENST00000522053.2:n.660G>T
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ENST00000523372.2:c.852G>T
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|
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ENST00000638552.1:c.484G>T
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ENSP00000491763.1:p.Gly162Ter
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ENST00000638660.1:c.484G>T
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ENSP00000492869.1:p.Gly162Ter
|
|
ENST00000638772.1:c.769G>T
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ENSP00000491557.1:p.Gly257Ter
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ENST00000638782.1:n.831G>T
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ENST00000638877.1:c.646G>T
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|
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ENST00000639046.1:c.160G>T
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ENSP00000492659.1:p.Gly54Ter
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ENST00000639111.2:c.769G>T
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ENSP00000492125.2:p.Gly257Ter
|
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ENST00000639213.2:c.769G>T
MANE Select
|
ENSP00000491909.2:p.Gly257Ter
|
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ENST00000639278.1:c.697G>T
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ENSP00000491958.1:p.Gly233Ter
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ENST00000639384.1:c.769G>T
|
ENSP00000491240.1:p.Gly257Ter
|
|
ENST00000639424.1:c.107+35920G>T
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ENSP00000491245.1:n.107+35920G>T
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|
ENST00000639683.1:c.703G>T
|
ENSP00000492581.1:p.Gly235Ter
|
|
ENST00000639975.1:c.703G>T
|
ENSP00000492096.1:p.Gly235Ter
|
|
ENST00000640574.1:c.484G>T
|
ENSP00000491582.1:p.Gly162Ter
|
|
ENST00000640739.1:n.3300G>T
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|
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ENST00000640910.1:c.207G>T
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|
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ENST00000640985.1:c.682G>T
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ENSP00000492293.1:p.Gly228Ter
|
|
ENST00000641017.1:c.769G>T
|
ENSP00000493461.1:p.Gly257Ter
|
|
ENST00000356592.7:c.769G>T
|
ENSP00000349000.3:p.Gly257Ter
|
|
ENST00000361925.8:c.769G>T
|
ENSP00000354651.4:p.Gly257Ter
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|
ENST00000414552.6:c.889G>T
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ENSP00000410732.2:p.Gly297Ter
|
|
ENST00000522053.1:c.484G>T
|
ENSP00000430182.1:p.Gly162Ter
|
|
ENST00000522990.5:c.*371G>T
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ENSP00000430732.1:n.*371G>T
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|
ENST00000523372.1:c.890G>T
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ENSP00000430124.1:n.890G>T
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|
NM_000816.3:c.769G>T
|
NP_000807.2:p.Gly257Ter
|
|
NM_198903.2:c.889G>T
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NP_944493.2:p.Gly297Ter
|
|
NM_198904.2:c.769G>T
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NP_944494.1:p.Gly257Ter
|
|
NM_001375339.1:c.760G>T
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NP_001362268.1:p.Gly254Ter
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|
NM_001375340.1:c.769G>T
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NP_001362269.1:p.Gly257Ter
|
|
NM_001375341.1:c.769G>T
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NP_001362270.1:p.Asp257Tyr
|
|
NM_001375342.1:c.769G>T
|
NP_001362271.1:p.Asp257Tyr
|
|
NM_001375343.1:c.889G>T
|
NP_001362272.1:p.Gly297Ter
|
|
NM_001375344.1:c.769G>T
|
NP_001362273.1:p.Glu257Ter
|
|
NM_001375345.1:c.703G>T
|
NP_001362274.1:p.Gly235Ter
|
|
NM_001375346.1:c.703G>T
|
NP_001362275.1:p.Gly235Ter
|
|
NM_001375347.1:c.682G>T
|
NP_001362276.1:p.Gly228Ter
|
|
NM_001375348.1:c.349G>T
|
NP_001362277.1:p.Gly117Ter
|
|
NM_001375349.1:c.484G>T
|
NP_001362278.1:p.Gly162Ter
|
|
NM_001375350.1:c.349G>T
|
NP_001362279.1:p.Gly117Ter
|
|
NM_198904.3:c.769G>T
|
NP_944494.1:p.Gly257Ter
|
|
NM_198904.4:c.769G>T
MANE Select
|
NP_944494.1:p.Gly257Ter
|
|