ENST00000269571.10:c.2360G>A
MANE Select
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ENSP00000269571.4:p.Gly787Asp
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ENST00000269571.9:c.2360G>A
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ENSP00000269571.4:p.Gly787Asp
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ENST00000406381.6:c.2270G>A
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ENSP00000385185.2:p.Gly757Asp
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ENST00000445658.6:c.1532G>A
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ENSP00000404047.2:p.Gly511Asp
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ENST00000541774.5:c.2315G>A
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ENSP00000446466.1:p.Gly772Asp
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ENST00000578373.5:c.*2150G>A
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ENSP00000463427.1:n.*2150G>A
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ENST00000580074.1:c.466G>A
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ENST00000583038.5:n.3494G>A
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ENST00000584450.5:c.2360G>A
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ENSP00000463714.1:p.Gly787Asp
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ENST00000584601.5:c.2270G>A
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ENSP00000462438.1:p.Gly757Asp
|
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NM_001005862.2:c.2270G>A , LRG_724t1:c.2270G>A
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NP_001005862.1:p.Gly757Asp
|
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NM_001289936.1:c.2315G>A , LRG_724t4:c.2315G>A
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NP_001276865.1:p.Gly772Asp
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NM_001289937.1:c.2360G>A
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NP_001276866.1:p.Gly787Asp
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NM_004448.3:c.2360G>A , LRG_724t2:c.2360G>A
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NP_004439.2:p.Gly787Asp
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NR_110535.1:n.2684G>A
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XM_024450641.1:c.2498G>A
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XP_024306409.1:p.Gly833Asp
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XM_024450642.1:c.2453G>A
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XP_024306410.1:p.Gly818Asp
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XM_024450643.1:c.2408G>A
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XP_024306411.1:p.Gly803Asp
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NM_001005862.3:c.2270G>A
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NP_001005862.1:p.Gly757Asp
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NM_001289936.2:c.2315G>A
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NP_001276865.1:p.Gly772Asp
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NM_001289937.2:c.2360G>A
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NP_001276866.1:p.Gly787Asp
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NM_001382782.1:c.2270G>A
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NP_001369711.1:p.Gly757Asp
|
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NM_001382783.1:c.2270G>A
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NP_001369712.1:p.Gly757Asp
|
|
NM_001382784.1:c.2477G>A
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NP_001369713.1:p.Gly826Asp
|
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NM_001382785.1:c.2462G>A
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NP_001369714.1:p.Gly821Asp
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NM_001382786.1:c.2441G>A
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NP_001369715.1:p.Gly814Asp
|
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NM_001382787.1:c.2435G>A
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NP_001369716.1:p.Gly812Asp
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NM_001382788.1:c.2390G>A
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NP_001369717.1:p.Gly797Asp
|
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NM_001382789.1:c.2381G>A
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NP_001369718.1:p.Gly794Asp
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NM_001382790.1:c.2357G>A
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NP_001369719.1:p.Gly786Asp
|
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NM_001382791.1:c.2351G>A
|
NP_001369720.1:p.Gly784Asp
|
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NM_001382792.1:c.2324G>A
|
NP_001369721.1:p.Gly775Asp
|
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NM_001382793.1:c.2318G>A
|
NP_001369722.1:p.Gly773Asp
|
|
NM_001382794.1:c.2318G>A
|
NP_001369723.1:p.Gly773Asp
|
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NM_001382795.1:c.2312G>A
|
NP_001369724.1:p.Gly771Asp
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|
NM_001382796.1:c.2360G>A
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NP_001369725.1:p.Gly787Asp
|
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NM_001382797.1:c.2261G>A
|
NP_001369726.1:p.Gly754Asp
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NM_001382798.1:c.2360G>A
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NP_001369727.1:p.Gly787Asp
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NM_001382799.1:c.2180G>A
|
NP_001369728.1:p.Gly727Asp
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NM_001382800.1:c.2308-271G>A
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NP_001369729.1:n.2308-271G>A
|
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NM_001382801.1:c.2312G>A
|
NP_001369730.1:p.Gly771Asp
|
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NM_001382802.1:c.2102G>A
|
NP_001369731.1:p.Gly701Asp
|
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NM_001382803.1:c.2318G>A
|
NP_001369732.1:p.Gly773Asp
|
|
NM_001382804.1:c.1532G>A
|
NP_001369733.1:p.Gly511Asp
|
|
NM_001382805.1:c.2208+1118G>A
|
NP_001369734.1:n.2208+1118G>A
|
|
NM_001382806.1:c.1322G>A
|
NP_001369735.1:p.Gly441Asp
|
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NM_004448.4:c.2360G>A
MANE Select
|
NP_004439.2:p.Gly787Asp
|
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NR_110535.2:n.2598G>A
|
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