ENST00000355699.7:c.1361A>G
MANE Select
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ENSP00000347927.2:p.Asp454Gly
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ENST00000355699.6:c.1361A>G
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ENSP00000347927.2:p.Asp454Gly
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ENST00000356589.6:c.1268A>G
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ENSP00000348997.2:p.Asp423Gly
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ENST00000371916.5:c.617A>G
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ENSP00000360984.2:p.Asp206Gly
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ENST00000371929.7:c.1361A>G
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ENSP00000360997.3:p.Asp454Gly
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ENST00000474918.1:c.*165A>G
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ENSP00000435305.1:n.*165A>G
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ENST00000485925.5:n.974-2485A>G
|
|
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ENST00000495234.5:c.*645A>G
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ENSP00000435274.1:n.*645A>G
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NM_139025.4:c.1361A>G , LRG_544t1:c.1361A>G
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NP_620594.1:p.Asp454Gly
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NM_139026.4:c.1268A>G
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NP_620595.1:p.Asp423Gly
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NM_139027.4:c.1361A>G
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NP_620596.2:p.Asp454Gly
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NR_024514.2:n.993-2485A>G
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|
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XM_011518174.1:c.971A>G
|
XP_011516476.1:p.Asp324Gly
|
|
XM_011518175.1:c.1361A>G
|
XP_011516477.1:p.Asp454Gly
|
|
XM_011518176.1:c.377A>G
|
XP_011516478.1:p.Asp126Gly
|
|
XM_011518177.1:c.371A>G
|
XP_011516479.1:p.Asp124Gly
|
|
XM_011518178.1:c.26A>G
|
XP_011516480.1:p.Asp9Gly
|
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XM_011518179.1:c.147A>G
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XP_011516481.1:p.Arg49=
|
|
XM_011518180.1:c.687-7982A>G
|
XP_011516482.1:n.687-7982A>G
|
|
XM_011518176.3:c.377A>G
|
XP_011516478.1:p.Asp126Gly
|
|
XM_011518178.2:c.26A>G
|
XP_011516480.1:p.Asp9Gly
|
|
XM_017014232.1:c.1349A>G
|
XP_016869721.1:p.Asp450Gly
|
|
XM_017014233.1:c.971A>G
|
XP_016869722.1:p.Asp324Gly
|
|
XM_017014234.2:c.371A>G
|
XP_016869723.1:p.Asp124Gly
|
|
XM_017014235.1:c.1361A>G
|
XP_016869724.1:p.Asp454Gly
|
|
XR_001746171.1:n.2586A>G
|
|
|
NM_139026.5:c.1268A>G
|
NP_620595.1:p.Asp423Gly
|
|
NM_139027.5:c.1361A>G
|
NP_620596.2:p.Asp454Gly
|
|
NM_139025.5:c.1361A>G
|
NP_620594.1:p.Asp454Gly
|
|
NM_139026.6:c.1268A>G
|
NP_620595.1:p.Asp423Gly
|
|
NM_139027.6:c.1361A>G
MANE Select
|
NP_620596.2:p.Asp454Gly
|
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NR_024514.3:n.995-2485A>G
|
|
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