ENST00000269571.10:c.2423A>T
MANE Select
|
ENSP00000269571.4:p.Asp808Val
|
|
ENST00000269571.9:c.2423A>T
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ENSP00000269571.4:p.Asp808Val
|
|
ENST00000406381.6:c.2333A>T
|
ENSP00000385185.2:p.Asp778Val
|
|
ENST00000445658.6:c.1595A>T
|
ENSP00000404047.2:p.Asp532Val
|
|
ENST00000541774.5:c.2378A>T
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ENSP00000446466.1:p.Asp793Val
|
|
ENST00000578373.5:c.*2213A>T
|
ENSP00000463427.1:n.*2213A>T
|
|
ENST00000580074.1:c.529A>T
|
|
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ENST00000583038.5:n.3557A>T
|
|
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ENST00000584450.5:c.2423A>T
|
ENSP00000463714.1:p.Asp808Val
|
|
ENST00000584601.5:c.2333A>T
|
ENSP00000462438.1:p.Asp778Val
|
|
NM_001005862.2:c.2333A>T , LRG_724t1:c.2333A>T
|
NP_001005862.1:p.Asp778Val
|
|
NM_001289936.1:c.2378A>T , LRG_724t4:c.2378A>T
|
NP_001276865.1:p.Asp793Val
|
|
NM_001289937.1:c.2423A>T
|
NP_001276866.1:p.Asp808Val
|
|
NM_004448.3:c.2423A>T , LRG_724t2:c.2423A>T
|
NP_004439.2:p.Asp808Val
|
|
NR_110535.1:n.2747A>T
|
|
|
XM_024450641.1:c.2561A>T
|
XP_024306409.1:p.Asp854Val
|
|
XM_024450642.1:c.2516A>T
|
XP_024306410.1:p.Asp839Val
|
|
XM_024450643.1:c.2471A>T
|
XP_024306411.1:p.Asp824Val
|
|
NM_001005862.3:c.2333A>T
|
NP_001005862.1:p.Asp778Val
|
|
NM_001289936.2:c.2378A>T
|
NP_001276865.1:p.Asp793Val
|
|
NM_001289937.2:c.2423A>T
|
NP_001276866.1:p.Asp808Val
|
|
NM_001382782.1:c.2333A>T
|
NP_001369711.1:p.Asp778Val
|
|
NM_001382783.1:c.2333A>T
|
NP_001369712.1:p.Asp778Val
|
|
NM_001382784.1:c.2540A>T
|
NP_001369713.1:p.Asp847Val
|
|
NM_001382785.1:c.2525A>T
|
NP_001369714.1:p.Asp842Val
|
|
NM_001382786.1:c.2504A>T
|
NP_001369715.1:p.Asp835Val
|
|
NM_001382787.1:c.2498A>T
|
NP_001369716.1:p.Asp833Val
|
|
NM_001382788.1:c.2453A>T
|
NP_001369717.1:p.Asp818Val
|
|
NM_001382789.1:c.2444A>T
|
NP_001369718.1:p.Asp815Val
|
|
NM_001382790.1:c.2420A>T
|
NP_001369719.1:p.Asp807Val
|
|
NM_001382791.1:c.2414A>T
|
NP_001369720.1:p.Asp805Val
|
|
NM_001382792.1:c.2387A>T
|
NP_001369721.1:p.Asp796Val
|
|
NM_001382793.1:c.2381A>T
|
NP_001369722.1:p.Asp794Val
|
|
NM_001382794.1:c.2381A>T
|
NP_001369723.1:p.Asp794Val
|
|
NM_001382795.1:c.2375A>T
|
NP_001369724.1:p.Asp792Val
|
|
NM_001382796.1:c.2423A>T
|
NP_001369725.1:p.Asp808Val
|
|
NM_001382797.1:c.2324A>T
|
NP_001369726.1:p.Asp775Val
|
|
NM_001382798.1:c.2423A>T
|
NP_001369727.1:p.Asp808Val
|
|
NM_001382799.1:c.2243A>T
|
NP_001369728.1:p.Asp748Val
|
|
NM_001382800.1:c.2308-208A>T
|
NP_001369729.1:n.2308-208A>T
|
|
NM_001382801.1:c.2375A>T
|
NP_001369730.1:p.Asp792Val
|
|
NM_001382802.1:c.2165A>T
|
NP_001369731.1:p.Asp722Val
|
|
NM_001382803.1:c.2381A>T
|
NP_001369732.1:p.Asp794Val
|
|
NM_001382804.1:c.1595A>T
|
NP_001369733.1:p.Asp532Val
|
|
NM_001382805.1:c.2208+1181A>T
|
NP_001369734.1:n.2208+1181A>T
|
|
NM_001382806.1:c.1385A>T
|
NP_001369735.1:p.Asp462Val
|
|
NM_004448.4:c.2423A>T
MANE Select
|
NP_004439.2:p.Asp808Val
|
|
NR_110535.2:n.2661A>T
|
|
|