|
ENST00000269571.10:c.2503T>G
MANE Select
|
ENSP00000269571.4:p.Tyr835Asp
|
|
|
ENST00000269571.9:c.2503T>G
|
ENSP00000269571.4:p.Tyr835Asp
|
|
|
ENST00000406381.6:c.2413T>G
|
ENSP00000385185.2:p.Tyr805Asp
|
|
|
ENST00000445658.6:c.1675T>G
|
ENSP00000404047.2:p.Tyr559Asp
|
|
|
ENST00000541774.5:c.2458T>G
|
ENSP00000446466.1:p.Tyr820Asp
|
|
|
ENST00000578373.5:c.*2293T>G
|
ENSP00000463427.1:n.*2293T>G
|
|
|
ENST00000580074.1:c.609T>G
|
|
|
|
ENST00000583038.5:n.3637T>G
|
|
|
|
ENST00000584450.5:c.2503T>G
|
ENSP00000463714.1:p.Tyr835Asp
|
|
|
ENST00000584601.5:c.2413T>G
|
ENSP00000462438.1:p.Tyr805Asp
|
|
|
NM_001005862.2:c.2413T>G , LRG_724t1:c.2413T>G
|
NP_001005862.1:p.Tyr805Asp
|
|
|
NM_001289936.1:c.2458T>G , LRG_724t4:c.2458T>G
|
NP_001276865.1:p.Tyr820Asp
|
|
|
NM_001289937.1:c.2503T>G
|
NP_001276866.1:p.Tyr835Asp
|
|
|
NM_004448.3:c.2503T>G , LRG_724t2:c.2503T>G
|
NP_004439.2:p.Tyr835Asp
|
|
|
NR_110535.1:n.2827T>G
|
|
|
|
XM_024450641.1:c.2641T>G
|
XP_024306409.1:p.Tyr881Asp
|
|
|
XM_024450642.1:c.2596T>G
|
XP_024306410.1:p.Tyr866Asp
|
|
|
XM_024450643.1:c.2551T>G
|
XP_024306411.1:p.Tyr851Asp
|
|
|
NM_001005862.3:c.2413T>G
|
NP_001005862.1:p.Tyr805Asp
|
|
|
NM_001289936.2:c.2458T>G
|
NP_001276865.1:p.Tyr820Asp
|
|
|
NM_001289937.2:c.2503T>G
|
NP_001276866.1:p.Tyr835Asp
|
|
|
NM_001382782.1:c.2413T>G
|
NP_001369711.1:p.Tyr805Asp
|
|
|
NM_001382783.1:c.2413T>G
|
NP_001369712.1:p.Tyr805Asp
|
|
|
NM_001382784.1:c.2620T>G
|
NP_001369713.1:p.Tyr874Asp
|
|
|
NM_001382785.1:c.2605T>G
|
NP_001369714.1:p.Tyr869Asp
|
|
|
NM_001382786.1:c.2584T>G
|
NP_001369715.1:p.Tyr862Asp
|
|
|
NM_001382787.1:c.2578T>G
|
NP_001369716.1:p.Tyr860Asp
|
|
|
NM_001382788.1:c.2533T>G
|
NP_001369717.1:p.Tyr845Asp
|
|
|
NM_001382789.1:c.2524T>G
|
NP_001369718.1:p.Tyr842Asp
|
|
|
NM_001382790.1:c.2500T>G
|
NP_001369719.1:p.Tyr834Asp
|
|
|
NM_001382791.1:c.2494T>G
|
NP_001369720.1:p.Tyr832Asp
|
|
|
NM_001382792.1:c.2467T>G
|
NP_001369721.1:p.Tyr823Asp
|
|
|
NM_001382793.1:c.2461T>G
|
NP_001369722.1:p.Tyr821Asp
|
|
|
NM_001382794.1:c.2461T>G
|
NP_001369723.1:p.Tyr821Asp
|
|
|
NM_001382795.1:c.2455T>G
|
NP_001369724.1:p.Tyr819Asp
|
|
|
NM_001382796.1:c.2503T>G
|
NP_001369725.1:p.Tyr835Asp
|
|
|
NM_001382797.1:c.2404T>G
|
NP_001369726.1:p.Tyr802Asp
|
|
|
NM_001382798.1:c.2493+147T>G
|
NP_001369727.1:n.2493+147T>G
|
|
|
NM_001382799.1:c.2323T>G
|
NP_001369728.1:p.Tyr775Asp
|
|
|
NM_001382800.1:c.2317T>G
|
NP_001369729.1:p.Tyr773Asp
|
|
|
NM_001382801.1:c.2445+147T>G
|
NP_001369730.1:n.2445+147T>G
|
|
|
NM_001382802.1:c.2245T>G
|
NP_001369731.1:p.Tyr749Asp
|
|
|
NM_001382803.1:c.2461T>G
|
NP_001369732.1:p.Tyr821Asp
|
|
|
NM_001382804.1:c.1675T>G
|
NP_001369733.1:p.Tyr559Asp
|
|
|
NM_001382805.1:c.2208+1398T>G
|
NP_001369734.1:n.2208+1398T>G
|
|
|
NM_001382806.1:c.1465T>G
|
NP_001369735.1:p.Tyr489Asp
|
|
|
NM_004448.4:c.2503T>G
MANE Select
|
NP_004439.2:p.Tyr835Asp
|
|
|
NR_110535.2:n.2741T>G
|
|
|
