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ENST00000269571.10:c.2415C>G
MANE Select
|
ENSP00000269571.4:p.Cys805Trp
|
|
|
ENST00000269571.9:c.2415C>G
|
ENSP00000269571.4:p.Cys805Trp
|
|
|
ENST00000406381.6:c.2325C>G
|
ENSP00000385185.2:p.Cys775Trp
|
|
|
ENST00000445658.6:c.1587C>G
|
ENSP00000404047.2:p.Cys529Trp
|
|
|
ENST00000541774.5:c.2370C>G
|
ENSP00000446466.1:p.Cys790Trp
|
|
|
ENST00000578373.5:c.*2205C>G
|
ENSP00000463427.1:n.*2205C>G
|
|
|
ENST00000580074.1:c.521C>G
|
|
|
|
ENST00000583038.5:n.3549C>G
|
|
|
|
ENST00000584450.5:c.2415C>G
|
ENSP00000463714.1:p.Cys805Trp
|
|
|
ENST00000584601.5:c.2325C>G
|
ENSP00000462438.1:p.Cys775Trp
|
|
|
NM_001005862.2:c.2325C>G , LRG_724t1:c.2325C>G
|
NP_001005862.1:p.Cys775Trp
|
|
|
NM_001289936.1:c.2370C>G , LRG_724t4:c.2370C>G
|
NP_001276865.1:p.Cys790Trp
|
|
|
NM_001289937.1:c.2415C>G
|
NP_001276866.1:p.Cys805Trp
|
|
|
NM_004448.3:c.2415C>G , LRG_724t2:c.2415C>G
|
NP_004439.2:p.Cys805Trp
|
|
|
NR_110535.1:n.2739C>G
|
|
|
|
XM_024450641.1:c.2553C>G
|
XP_024306409.1:p.Cys851Trp
|
|
|
XM_024450642.1:c.2508C>G
|
XP_024306410.1:p.Cys836Trp
|
|
|
XM_024450643.1:c.2463C>G
|
XP_024306411.1:p.Cys821Trp
|
|
|
NM_001005862.3:c.2325C>G
|
NP_001005862.1:p.Cys775Trp
|
|
|
NM_001289936.2:c.2370C>G
|
NP_001276865.1:p.Cys790Trp
|
|
|
NM_001289937.2:c.2415C>G
|
NP_001276866.1:p.Cys805Trp
|
|
|
NM_001382782.1:c.2325C>G
|
NP_001369711.1:p.Cys775Trp
|
|
|
NM_001382783.1:c.2325C>G
|
NP_001369712.1:p.Cys775Trp
|
|
|
NM_001382784.1:c.2532C>G
|
NP_001369713.1:p.Cys844Trp
|
|
|
NM_001382785.1:c.2517C>G
|
NP_001369714.1:p.Cys839Trp
|
|
|
NM_001382786.1:c.2496C>G
|
NP_001369715.1:p.Cys832Trp
|
|
|
NM_001382787.1:c.2490C>G
|
NP_001369716.1:p.Cys830Trp
|
|
|
NM_001382788.1:c.2445C>G
|
NP_001369717.1:p.Cys815Trp
|
|
|
NM_001382789.1:c.2436C>G
|
NP_001369718.1:p.Cys812Trp
|
|
|
NM_001382790.1:c.2412C>G
|
NP_001369719.1:p.Cys804Trp
|
|
|
NM_001382791.1:c.2406C>G
|
NP_001369720.1:p.Cys802Trp
|
|
|
NM_001382792.1:c.2379C>G
|
NP_001369721.1:p.Cys793Trp
|
|
|
NM_001382793.1:c.2373C>G
|
NP_001369722.1:p.Cys791Trp
|
|
|
NM_001382794.1:c.2373C>G
|
NP_001369723.1:p.Cys791Trp
|
|
|
NM_001382795.1:c.2367C>G
|
NP_001369724.1:p.Cys789Trp
|
|
|
NM_001382796.1:c.2415C>G
|
NP_001369725.1:p.Cys805Trp
|
|
|
NM_001382797.1:c.2316C>G
|
NP_001369726.1:p.Cys772Trp
|
|
|
NM_001382798.1:c.2415C>G
|
NP_001369727.1:p.Cys805Trp
|
|
|
NM_001382799.1:c.2235C>G
|
NP_001369728.1:p.Cys745Trp
|
|
|
NM_001382800.1:c.2308-216C>G
|
NP_001369729.1:n.2308-216C>G
|
|
|
NM_001382801.1:c.2367C>G
|
NP_001369730.1:p.Cys789Trp
|
|
|
NM_001382802.1:c.2157C>G
|
NP_001369731.1:p.Cys719Trp
|
|
|
NM_001382803.1:c.2373C>G
|
NP_001369732.1:p.Cys791Trp
|
|
|
NM_001382804.1:c.1587C>G
|
NP_001369733.1:p.Cys529Trp
|
|
|
NM_001382805.1:c.2208+1173C>G
|
NP_001369734.1:n.2208+1173C>G
|
|
|
NM_001382806.1:c.1377C>G
|
NP_001369735.1:p.Cys459Trp
|
|
|
NM_004448.4:c.2415C>G
MANE Select
|
NP_004439.2:p.Cys805Trp
|
|
|
NR_110535.2:n.2653C>G
|
|
|
