ENST00000269571.10:c.2531G>T
MANE Select
|
ENSP00000269571.4:p.Arg844Met
|
|
ENST00000269571.9:c.2531G>T
|
ENSP00000269571.4:p.Arg844Met
|
|
ENST00000406381.6:c.2441G>T
|
ENSP00000385185.2:p.Arg814Met
|
|
ENST00000445658.6:c.1703G>T
|
ENSP00000404047.2:p.Arg568Met
|
|
ENST00000541774.5:c.2486G>T
|
ENSP00000446466.1:p.Arg829Met
|
|
ENST00000578373.5:c.*2321G>T
|
ENSP00000463427.1:n.*2321G>T
|
|
ENST00000580074.1:c.637G>T
|
|
|
ENST00000583038.5:n.3665G>T
|
|
|
ENST00000584450.5:c.2531G>T
|
ENSP00000463714.1:p.Arg844Met
|
|
ENST00000584601.5:c.2441G>T
|
ENSP00000462438.1:p.Arg814Met
|
|
NM_001005862.2:c.2441G>T , LRG_724t1:c.2441G>T
|
NP_001005862.1:p.Arg814Met
|
|
NM_001289936.1:c.2486G>T , LRG_724t4:c.2486G>T
|
NP_001276865.1:p.Arg829Met
|
|
NM_001289937.1:c.2531G>T
|
NP_001276866.1:p.Arg844Met
|
|
NM_004448.3:c.2531G>T , LRG_724t2:c.2531G>T
|
NP_004439.2:p.Arg844Met
|
|
NR_110535.1:n.2855G>T
|
|
|
XM_024450641.1:c.2669G>T
|
XP_024306409.1:p.Arg890Met
|
|
XM_024450642.1:c.2624G>T
|
XP_024306410.1:p.Arg875Met
|
|
XM_024450643.1:c.2579G>T
|
XP_024306411.1:p.Arg860Met
|
|
NM_001005862.3:c.2441G>T
|
NP_001005862.1:p.Arg814Met
|
|
NM_001289936.2:c.2486G>T
|
NP_001276865.1:p.Arg829Met
|
|
NM_001289937.2:c.2531G>T
|
NP_001276866.1:p.Arg844Met
|
|
NM_001382782.1:c.2441G>T
|
NP_001369711.1:p.Arg814Met
|
|
NM_001382783.1:c.2441G>T
|
NP_001369712.1:p.Arg814Met
|
|
NM_001382784.1:c.2648G>T
|
NP_001369713.1:p.Arg883Met
|
|
NM_001382785.1:c.2633G>T
|
NP_001369714.1:p.Arg878Met
|
|
NM_001382786.1:c.2612G>T
|
NP_001369715.1:p.Arg871Met
|
|
NM_001382787.1:c.2606G>T
|
NP_001369716.1:p.Arg869Met
|
|
NM_001382788.1:c.2561G>T
|
NP_001369717.1:p.Arg854Met
|
|
NM_001382789.1:c.2552G>T
|
NP_001369718.1:p.Arg851Met
|
|
NM_001382790.1:c.2528G>T
|
NP_001369719.1:p.Arg843Met
|
|
NM_001382791.1:c.2522G>T
|
NP_001369720.1:p.Arg841Met
|
|
NM_001382792.1:c.2495G>T
|
NP_001369721.1:p.Arg832Met
|
|
NM_001382793.1:c.2489G>T
|
NP_001369722.1:p.Arg830Met
|
|
NM_001382794.1:c.2489G>T
|
NP_001369723.1:p.Arg830Met
|
|
NM_001382795.1:c.2483G>T
|
NP_001369724.1:p.Arg828Met
|
|
NM_001382796.1:c.2531G>T
|
NP_001369725.1:p.Arg844Met
|
|
NM_001382797.1:c.2432G>T
|
NP_001369726.1:p.Arg811Met
|
|
NM_001382798.1:c.2493+175G>T
|
NP_001369727.1:n.2493+175G>T
|
|
NM_001382799.1:c.2351G>T
|
NP_001369728.1:p.Arg784Met
|
|
NM_001382800.1:c.2345G>T
|
NP_001369729.1:p.Arg782Met
|
|
NM_001382801.1:c.2445+175G>T
|
NP_001369730.1:n.2445+175G>T
|
|
NM_001382802.1:c.2273G>T
|
NP_001369731.1:p.Arg758Met
|
|
NM_001382803.1:c.2489G>T
|
NP_001369732.1:p.Arg830Met
|
|
NM_001382804.1:c.1703G>T
|
NP_001369733.1:p.Arg568Met
|
|
NM_001382805.1:c.2208+1426G>T
|
NP_001369734.1:n.2208+1426G>T
|
|
NM_001382806.1:c.1493G>T
|
NP_001369735.1:p.Arg498Met
|
|
NM_004448.4:c.2531G>T
MANE Select
|
NP_004439.2:p.Arg844Met
|
|
NR_110535.2:n.2769G>T
|
|
|