|
ENST00000269571.10:c.2381T>G
MANE Select
|
ENSP00000269571.4:p.Val794Gly
|
|
|
ENST00000269571.9:c.2381T>G
|
ENSP00000269571.4:p.Val794Gly
|
|
|
ENST00000406381.6:c.2291T>G
|
ENSP00000385185.2:p.Val764Gly
|
|
|
ENST00000445658.6:c.1553T>G
|
ENSP00000404047.2:p.Val518Gly
|
|
|
ENST00000541774.5:c.2336T>G
|
ENSP00000446466.1:p.Val779Gly
|
|
|
ENST00000578373.5:c.*2171T>G
|
ENSP00000463427.1:n.*2171T>G
|
|
|
ENST00000580074.1:c.487T>G
|
|
|
|
ENST00000583038.5:n.3515T>G
|
|
|
|
ENST00000584450.5:c.2381T>G
|
ENSP00000463714.1:p.Val794Gly
|
|
|
ENST00000584601.5:c.2291T>G
|
ENSP00000462438.1:p.Val764Gly
|
|
|
NM_001005862.2:c.2291T>G , LRG_724t1:c.2291T>G
|
NP_001005862.1:p.Val764Gly
|
|
|
NM_001289936.1:c.2336T>G , LRG_724t4:c.2336T>G
|
NP_001276865.1:p.Val779Gly
|
|
|
NM_001289937.1:c.2381T>G
|
NP_001276866.1:p.Val794Gly
|
|
|
NM_004448.3:c.2381T>G , LRG_724t2:c.2381T>G
|
NP_004439.2:p.Val794Gly
|
|
|
NR_110535.1:n.2705T>G
|
|
|
|
XM_024450641.1:c.2519T>G
|
XP_024306409.1:p.Val840Gly
|
|
|
XM_024450642.1:c.2474T>G
|
XP_024306410.1:p.Val825Gly
|
|
|
XM_024450643.1:c.2429T>G
|
XP_024306411.1:p.Val810Gly
|
|
|
NM_001005862.3:c.2291T>G
|
NP_001005862.1:p.Val764Gly
|
|
|
NM_001289936.2:c.2336T>G
|
NP_001276865.1:p.Val779Gly
|
|
|
NM_001289937.2:c.2381T>G
|
NP_001276866.1:p.Val794Gly
|
|
|
NM_001382782.1:c.2291T>G
|
NP_001369711.1:p.Val764Gly
|
|
|
NM_001382783.1:c.2291T>G
|
NP_001369712.1:p.Val764Gly
|
|
|
NM_001382784.1:c.2498T>G
|
NP_001369713.1:p.Val833Gly
|
|
|
NM_001382785.1:c.2483T>G
|
NP_001369714.1:p.Val828Gly
|
|
|
NM_001382786.1:c.2462T>G
|
NP_001369715.1:p.Val821Gly
|
|
|
NM_001382787.1:c.2456T>G
|
NP_001369716.1:p.Val819Gly
|
|
|
NM_001382788.1:c.2411T>G
|
NP_001369717.1:p.Val804Gly
|
|
|
NM_001382789.1:c.2402T>G
|
NP_001369718.1:p.Val801Gly
|
|
|
NM_001382790.1:c.2378T>G
|
NP_001369719.1:p.Val793Gly
|
|
|
NM_001382791.1:c.2372T>G
|
NP_001369720.1:p.Val791Gly
|
|
|
NM_001382792.1:c.2345T>G
|
NP_001369721.1:p.Val782Gly
|
|
|
NM_001382793.1:c.2339T>G
|
NP_001369722.1:p.Val780Gly
|
|
|
NM_001382794.1:c.2339T>G
|
NP_001369723.1:p.Val780Gly
|
|
|
NM_001382795.1:c.2333T>G
|
NP_001369724.1:p.Val778Gly
|
|
|
NM_001382796.1:c.2381T>G
|
NP_001369725.1:p.Val794Gly
|
|
|
NM_001382797.1:c.2282T>G
|
NP_001369726.1:p.Val761Gly
|
|
|
NM_001382798.1:c.2381T>G
|
NP_001369727.1:p.Val794Gly
|
|
|
NM_001382799.1:c.2201T>G
|
NP_001369728.1:p.Val734Gly
|
|
|
NM_001382800.1:c.2308-250T>G
|
NP_001369729.1:n.2308-250T>G
|
|
|
NM_001382801.1:c.2333T>G
|
NP_001369730.1:p.Val778Gly
|
|
|
NM_001382802.1:c.2123T>G
|
NP_001369731.1:p.Val708Gly
|
|
|
NM_001382803.1:c.2339T>G
|
NP_001369732.1:p.Val780Gly
|
|
|
NM_001382804.1:c.1553T>G
|
NP_001369733.1:p.Val518Gly
|
|
|
NM_001382805.1:c.2208+1139T>G
|
NP_001369734.1:n.2208+1139T>G
|
|
|
NM_001382806.1:c.1343T>G
|
NP_001369735.1:p.Val448Gly
|
|
|
NM_004448.4:c.2381T>G
MANE Select
|
NP_004439.2:p.Val794Gly
|
|
|
NR_110535.2:n.2619T>G
|
|
|
