ENST00000265909.9:c.2664A>G
MANE Select
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ENSP00000265909.4:p.Gly888=
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ENST00000265909.8:c.2664A>G
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ENSP00000265909.4:p.Gly888=
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ENST00000426933.6:c.168A>G
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ENSP00000413345.2:p.Gly56=
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ENST00000526579.5:n.178-1005A>G
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ENST00000527116.5:n.426A>G
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ENST00000528555.5:c.804A>G
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ENSP00000435122.1:p.Gly268=
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ENST00000530330.1:n.400A>G
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ENST00000530356.5:c.804A>G
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ENSP00000432307.1:p.Gly268=
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ENST00000533318.5:n.1024A>G
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ENST00000534726.5:c.384A>G
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ENSP00000433699.1:p.Gly128=
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NM_001301089.1:c.804A>G
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NP_001288018.1:p.Gly268=
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NM_014758.2:c.2664A>G
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NP_055573.2:p.Gly888=
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XM_005271546.3:c.2574-1005A>G
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XP_005271603.1:n.2574-1005A>G
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XM_011542819.1:c.2910A>G
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XP_011541121.1:p.Gly970=
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XM_011542820.1:c.2898A>G
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XP_011541122.1:p.Gly966=
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XM_011542821.1:c.2790A>G
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XP_011541123.1:p.Gly930=
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XM_011542824.1:c.2028A>G
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XP_011541126.1:p.Gly676=
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XM_011542825.1:c.1185A>G
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XP_011541127.1:p.Gly395=
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XM_011542826.1:c.1050A>G
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XP_011541128.1:p.Gly350=
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XM_011542827.1:c.930A>G
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XP_011541129.1:p.Gly310=
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NM_001347918.1:c.2544A>G
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NP_001334847.1:p.Gly848=
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NM_001347919.1:c.2574-1005A>G
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NP_001334848.1:n.2574-1005A>G
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NM_001347922.1:c.993A>G
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NP_001334851.1:p.Gly331=
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NM_001347923.1:c.939A>G
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NP_001334852.1:p.Gly313=
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NM_001347924.1:c.684A>G
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NP_001334853.1:p.Gly228=
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NM_001347925.1:c.630A>G
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NP_001334854.1:p.Gly210=
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NM_001347926.1:c.714-1005A>G
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NP_001334855.1:n.714-1005A>G
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NM_001347927.1:c.384A>G
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NP_001334856.1:p.Gly128=
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NR_144939.1:n.3297A>G
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XM_011542820.2:c.2898A>G
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XP_011541122.1:p.Gly966=
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XM_011542821.3:c.2790A>G
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XP_011541123.1:p.Gly930=
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XM_011542824.2:c.2028A>G
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XP_011541126.1:p.Gly676=
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XM_011542825.2:c.1185A>G
|
XP_011541127.1:p.Gly395=
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XM_011542826.2:c.1050A>G
|
XP_011541128.1:p.Gly350=
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XM_024448521.1:c.2910A>G
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XP_024304289.1:p.Gly970=
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XR_001747870.1:n.3735A>G
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XR_001747872.1:n.3081A>G
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XR_001747873.1:n.3395A>G
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NM_001301089.2:c.804A>G
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NP_001288018.1:p.Gly268=
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NM_001347918.2:c.2544A>G
|
NP_001334847.2:p.Gly848=
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NM_001347919.2:c.2574-1005A>G
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NP_001334848.2:n.2574-1005A>G
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NM_001347920.2:c.*21060A>G
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NP_001334849.2:n.*21060A>G
|
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NM_001347922.2:c.993A>G
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NP_001334851.2:p.Gly331=
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|
NM_001347923.2:c.939A>G
|
NP_001334852.2:p.Gly313=
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|
NM_001347924.2:c.684A>G
|
NP_001334853.1:p.Gly228=
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|
NM_001347925.2:c.630A>G
|
NP_001334854.1:p.Gly210=
|
|
NM_001347926.2:c.714-1005A>G
|
NP_001334855.1:n.714-1005A>G
|
|
NM_001347927.2:c.384A>G
|
NP_001334856.1:p.Gly128=
|
|
NM_014758.3:c.2664A>G
MANE Select
|
NP_055573.3:p.Gly888=
|
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NR_144939.2:n.3289A>G
|
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