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ENST00000269571.10:c.2514T>G
MANE Select
|
ENSP00000269571.4:p.Asp838Glu
|
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ENST00000269571.9:c.2514T>G
|
ENSP00000269571.4:p.Asp838Glu
|
|
|
ENST00000406381.6:c.2424T>G
|
ENSP00000385185.2:p.Asp808Glu
|
|
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ENST00000445658.6:c.1686T>G
|
ENSP00000404047.2:p.Asp562Glu
|
|
|
ENST00000541774.5:c.2469T>G
|
ENSP00000446466.1:p.Asp823Glu
|
|
|
ENST00000578373.5:c.*2304T>G
|
ENSP00000463427.1:n.*2304T>G
|
|
|
ENST00000580074.1:c.620T>G
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|
|
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ENST00000583038.5:n.3648T>G
|
|
|
|
ENST00000584450.5:c.2514T>G
|
ENSP00000463714.1:p.Asp838Glu
|
|
|
ENST00000584601.5:c.2424T>G
|
ENSP00000462438.1:p.Asp808Glu
|
|
|
NM_001005862.2:c.2424T>G , LRG_724t1:c.2424T>G
|
NP_001005862.1:p.Asp808Glu
|
|
|
NM_001289936.1:c.2469T>G , LRG_724t4:c.2469T>G
|
NP_001276865.1:p.Asp823Glu
|
|
|
NM_001289937.1:c.2514T>G
|
NP_001276866.1:p.Asp838Glu
|
|
|
NM_004448.3:c.2514T>G , LRG_724t2:c.2514T>G
|
NP_004439.2:p.Asp838Glu
|
|
|
NR_110535.1:n.2838T>G
|
|
|
|
XM_024450641.1:c.2652T>G
|
XP_024306409.1:p.Asp884Glu
|
|
|
XM_024450642.1:c.2607T>G
|
XP_024306410.1:p.Asp869Glu
|
|
|
XM_024450643.1:c.2562T>G
|
XP_024306411.1:p.Asp854Glu
|
|
|
NM_001005862.3:c.2424T>G
|
NP_001005862.1:p.Asp808Glu
|
|
|
NM_001289936.2:c.2469T>G
|
NP_001276865.1:p.Asp823Glu
|
|
|
NM_001289937.2:c.2514T>G
|
NP_001276866.1:p.Asp838Glu
|
|
|
NM_001382782.1:c.2424T>G
|
NP_001369711.1:p.Asp808Glu
|
|
|
NM_001382783.1:c.2424T>G
|
NP_001369712.1:p.Asp808Glu
|
|
|
NM_001382784.1:c.2631T>G
|
NP_001369713.1:p.Asp877Glu
|
|
|
NM_001382785.1:c.2616T>G
|
NP_001369714.1:p.Asp872Glu
|
|
|
NM_001382786.1:c.2595T>G
|
NP_001369715.1:p.Asp865Glu
|
|
|
NM_001382787.1:c.2589T>G
|
NP_001369716.1:p.Asp863Glu
|
|
|
NM_001382788.1:c.2544T>G
|
NP_001369717.1:p.Asp848Glu
|
|
|
NM_001382789.1:c.2535T>G
|
NP_001369718.1:p.Asp845Glu
|
|
|
NM_001382790.1:c.2511T>G
|
NP_001369719.1:p.Asp837Glu
|
|
|
NM_001382791.1:c.2505T>G
|
NP_001369720.1:p.Asp835Glu
|
|
|
NM_001382792.1:c.2478T>G
|
NP_001369721.1:p.Asp826Glu
|
|
|
NM_001382793.1:c.2472T>G
|
NP_001369722.1:p.Asp824Glu
|
|
|
NM_001382794.1:c.2472T>G
|
NP_001369723.1:p.Asp824Glu
|
|
|
NM_001382795.1:c.2466T>G
|
NP_001369724.1:p.Asp822Glu
|
|
|
NM_001382796.1:c.2514T>G
|
NP_001369725.1:p.Asp838Glu
|
|
|
NM_001382797.1:c.2415T>G
|
NP_001369726.1:p.Asp805Glu
|
|
|
NM_001382798.1:c.2493+158T>G
|
NP_001369727.1:n.2493+158T>G
|
|
|
NM_001382799.1:c.2334T>G
|
NP_001369728.1:p.Asp778Glu
|
|
|
NM_001382800.1:c.2328T>G
|
NP_001369729.1:p.Asp776Glu
|
|
|
NM_001382801.1:c.2445+158T>G
|
NP_001369730.1:n.2445+158T>G
|
|
|
NM_001382802.1:c.2256T>G
|
NP_001369731.1:p.Asp752Glu
|
|
|
NM_001382803.1:c.2472T>G
|
NP_001369732.1:p.Asp824Glu
|
|
|
NM_001382804.1:c.1686T>G
|
NP_001369733.1:p.Asp562Glu
|
|
|
NM_001382805.1:c.2208+1409T>G
|
NP_001369734.1:n.2208+1409T>G
|
|
|
NM_001382806.1:c.1476T>G
|
NP_001369735.1:p.Asp492Glu
|
|
|
NM_004448.4:c.2514T>G
MANE Select
|
NP_004439.2:p.Asp838Glu
|
|
|
NR_110535.2:n.2752T>G
|
|
|
