|
ENST00000269571.10:c.2341T>G
MANE Select
|
ENSP00000269571.4:p.Tyr781Asp
|
|
|
ENST00000269571.9:c.2341T>G
|
ENSP00000269571.4:p.Tyr781Asp
|
|
|
ENST00000406381.6:c.2251T>G
|
ENSP00000385185.2:p.Tyr751Asp
|
|
|
ENST00000445658.6:c.1513T>G
|
ENSP00000404047.2:p.Tyr505Asp
|
|
|
ENST00000541774.5:c.2296T>G
|
ENSP00000446466.1:p.Tyr766Asp
|
|
|
ENST00000578373.5:c.*2131T>G
|
ENSP00000463427.1:n.*2131T>G
|
|
|
ENST00000580074.1:c.447T>G
|
|
|
|
ENST00000583038.5:n.3475T>G
|
|
|
|
ENST00000584450.5:c.2341T>G
|
ENSP00000463714.1:p.Tyr781Asp
|
|
|
ENST00000584601.5:c.2251T>G
|
ENSP00000462438.1:p.Tyr751Asp
|
|
|
NM_001005862.2:c.2251T>G , LRG_724t1:c.2251T>G
|
NP_001005862.1:p.Tyr751Asp
|
|
|
NM_001289936.1:c.2296T>G , LRG_724t4:c.2296T>G
|
NP_001276865.1:p.Tyr766Asp
|
|
|
NM_001289937.1:c.2341T>G
|
NP_001276866.1:p.Tyr781Asp
|
|
|
NM_004448.3:c.2341T>G , LRG_724t2:c.2341T>G
|
NP_004439.2:p.Tyr781Asp
|
|
|
NR_110535.1:n.2665T>G
|
|
|
|
XM_024450641.1:c.2479T>G
|
XP_024306409.1:p.Tyr827Asp
|
|
|
XM_024450642.1:c.2434T>G
|
XP_024306410.1:p.Tyr812Asp
|
|
|
XM_024450643.1:c.2389T>G
|
XP_024306411.1:p.Tyr797Asp
|
|
|
NM_001005862.3:c.2251T>G
|
NP_001005862.1:p.Tyr751Asp
|
|
|
NM_001289936.2:c.2296T>G
|
NP_001276865.1:p.Tyr766Asp
|
|
|
NM_001289937.2:c.2341T>G
|
NP_001276866.1:p.Tyr781Asp
|
|
|
NM_001382782.1:c.2251T>G
|
NP_001369711.1:p.Tyr751Asp
|
|
|
NM_001382783.1:c.2251T>G
|
NP_001369712.1:p.Tyr751Asp
|
|
|
NM_001382784.1:c.2458T>G
|
NP_001369713.1:p.Tyr820Asp
|
|
|
NM_001382785.1:c.2443T>G
|
NP_001369714.1:p.Tyr815Asp
|
|
|
NM_001382786.1:c.2422T>G
|
NP_001369715.1:p.Tyr808Asp
|
|
|
NM_001382787.1:c.2416T>G
|
NP_001369716.1:p.Tyr806Asp
|
|
|
NM_001382788.1:c.2371T>G
|
NP_001369717.1:p.Tyr791Asp
|
|
|
NM_001382789.1:c.2362T>G
|
NP_001369718.1:p.Tyr788Asp
|
|
|
NM_001382790.1:c.2338T>G
|
NP_001369719.1:p.Tyr780Asp
|
|
|
NM_001382791.1:c.2332T>G
|
NP_001369720.1:p.Tyr778Asp
|
|
|
NM_001382792.1:c.2305T>G
|
NP_001369721.1:p.Tyr769Asp
|
|
|
NM_001382793.1:c.2299T>G
|
NP_001369722.1:p.Tyr767Asp
|
|
|
NM_001382794.1:c.2299T>G
|
NP_001369723.1:p.Tyr767Asp
|
|
|
NM_001382795.1:c.2293T>G
|
NP_001369724.1:p.Tyr765Asp
|
|
|
NM_001382796.1:c.2341T>G
|
NP_001369725.1:p.Tyr781Asp
|
|
|
NM_001382797.1:c.2242T>G
|
NP_001369726.1:p.Tyr748Asp
|
|
|
NM_001382798.1:c.2341T>G
|
NP_001369727.1:p.Tyr781Asp
|
|
|
NM_001382799.1:c.2161T>G
|
NP_001369728.1:p.Tyr721Asp
|
|
|
NM_001382800.1:c.2308-290T>G
|
NP_001369729.1:n.2308-290T>G
|
|
|
NM_001382801.1:c.2293T>G
|
NP_001369730.1:p.Tyr765Asp
|
|
|
NM_001382802.1:c.2083T>G
|
NP_001369731.1:p.Tyr695Asp
|
|
|
NM_001382803.1:c.2299T>G
|
NP_001369732.1:p.Tyr767Asp
|
|
|
NM_001382804.1:c.1513T>G
|
NP_001369733.1:p.Tyr505Asp
|
|
|
NM_001382805.1:c.2208+1099T>G
|
NP_001369734.1:n.2208+1099T>G
|
|
|
NM_001382806.1:c.1303T>G
|
NP_001369735.1:p.Tyr435Asp
|
|
|
NM_004448.4:c.2341T>G
MANE Select
|
NP_004439.2:p.Tyr781Asp
|
|
|
NR_110535.2:n.2579T>G
|
|
|
