|
ENST00000269571.10:c.2407T>G
MANE Select
|
ENSP00000269571.4:p.Tyr803Asp
|
|
|
ENST00000269571.9:c.2407T>G
|
ENSP00000269571.4:p.Tyr803Asp
|
|
|
ENST00000406381.6:c.2317T>G
|
ENSP00000385185.2:p.Tyr773Asp
|
|
|
ENST00000445658.6:c.1579T>G
|
ENSP00000404047.2:p.Tyr527Asp
|
|
|
ENST00000541774.5:c.2362T>G
|
ENSP00000446466.1:p.Tyr788Asp
|
|
|
ENST00000578373.5:c.*2197T>G
|
ENSP00000463427.1:n.*2197T>G
|
|
|
ENST00000580074.1:c.513T>G
|
|
|
|
ENST00000583038.5:n.3541T>G
|
|
|
|
ENST00000584450.5:c.2407T>G
|
ENSP00000463714.1:p.Tyr803Asp
|
|
|
ENST00000584601.5:c.2317T>G
|
ENSP00000462438.1:p.Tyr773Asp
|
|
|
NM_001005862.2:c.2317T>G , LRG_724t1:c.2317T>G
|
NP_001005862.1:p.Tyr773Asp
|
|
|
NM_001289936.1:c.2362T>G , LRG_724t4:c.2362T>G
|
NP_001276865.1:p.Tyr788Asp
|
|
|
NM_001289937.1:c.2407T>G
|
NP_001276866.1:p.Tyr803Asp
|
|
|
NM_004448.3:c.2407T>G , LRG_724t2:c.2407T>G
|
NP_004439.2:p.Tyr803Asp
|
|
|
NR_110535.1:n.2731T>G
|
|
|
|
XM_024450641.1:c.2545T>G
|
XP_024306409.1:p.Tyr849Asp
|
|
|
XM_024450642.1:c.2500T>G
|
XP_024306410.1:p.Tyr834Asp
|
|
|
XM_024450643.1:c.2455T>G
|
XP_024306411.1:p.Tyr819Asp
|
|
|
NM_001005862.3:c.2317T>G
|
NP_001005862.1:p.Tyr773Asp
|
|
|
NM_001289936.2:c.2362T>G
|
NP_001276865.1:p.Tyr788Asp
|
|
|
NM_001289937.2:c.2407T>G
|
NP_001276866.1:p.Tyr803Asp
|
|
|
NM_001382782.1:c.2317T>G
|
NP_001369711.1:p.Tyr773Asp
|
|
|
NM_001382783.1:c.2317T>G
|
NP_001369712.1:p.Tyr773Asp
|
|
|
NM_001382784.1:c.2524T>G
|
NP_001369713.1:p.Tyr842Asp
|
|
|
NM_001382785.1:c.2509T>G
|
NP_001369714.1:p.Tyr837Asp
|
|
|
NM_001382786.1:c.2488T>G
|
NP_001369715.1:p.Tyr830Asp
|
|
|
NM_001382787.1:c.2482T>G
|
NP_001369716.1:p.Tyr828Asp
|
|
|
NM_001382788.1:c.2437T>G
|
NP_001369717.1:p.Tyr813Asp
|
|
|
NM_001382789.1:c.2428T>G
|
NP_001369718.1:p.Tyr810Asp
|
|
|
NM_001382790.1:c.2404T>G
|
NP_001369719.1:p.Tyr802Asp
|
|
|
NM_001382791.1:c.2398T>G
|
NP_001369720.1:p.Tyr800Asp
|
|
|
NM_001382792.1:c.2371T>G
|
NP_001369721.1:p.Tyr791Asp
|
|
|
NM_001382793.1:c.2365T>G
|
NP_001369722.1:p.Tyr789Asp
|
|
|
NM_001382794.1:c.2365T>G
|
NP_001369723.1:p.Tyr789Asp
|
|
|
NM_001382795.1:c.2359T>G
|
NP_001369724.1:p.Tyr787Asp
|
|
|
NM_001382796.1:c.2407T>G
|
NP_001369725.1:p.Tyr803Asp
|
|
|
NM_001382797.1:c.2308T>G
|
NP_001369726.1:p.Tyr770Asp
|
|
|
NM_001382798.1:c.2407T>G
|
NP_001369727.1:p.Tyr803Asp
|
|
|
NM_001382799.1:c.2227T>G
|
NP_001369728.1:p.Tyr743Asp
|
|
|
NM_001382800.1:c.2308-224T>G
|
NP_001369729.1:n.2308-224T>G
|
|
|
NM_001382801.1:c.2359T>G
|
NP_001369730.1:p.Tyr787Asp
|
|
|
NM_001382802.1:c.2149T>G
|
NP_001369731.1:p.Tyr717Asp
|
|
|
NM_001382803.1:c.2365T>G
|
NP_001369732.1:p.Tyr789Asp
|
|
|
NM_001382804.1:c.1579T>G
|
NP_001369733.1:p.Tyr527Asp
|
|
|
NM_001382805.1:c.2208+1165T>G
|
NP_001369734.1:n.2208+1165T>G
|
|
|
NM_001382806.1:c.1369T>G
|
NP_001369735.1:p.Tyr457Asp
|
|
|
NM_004448.4:c.2407T>G
MANE Select
|
NP_004439.2:p.Tyr803Asp
|
|
|
NR_110535.2:n.2645T>G
|
|
|
