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ENST00000269571.10:c.2396A>G
MANE Select
|
ENSP00000269571.4:p.Gln799Arg
|
|
|
ENST00000269571.9:c.2396A>G
|
ENSP00000269571.4:p.Gln799Arg
|
|
|
ENST00000406381.6:c.2306A>G
|
ENSP00000385185.2:p.Gln769Arg
|
|
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ENST00000445658.6:c.1568A>G
|
ENSP00000404047.2:p.Gln523Arg
|
|
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ENST00000541774.5:c.2351A>G
|
ENSP00000446466.1:p.Gln784Arg
|
|
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ENST00000578373.5:c.*2186A>G
|
ENSP00000463427.1:n.*2186A>G
|
|
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ENST00000580074.1:c.502A>G
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ENST00000583038.5:n.3530A>G
|
|
|
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ENST00000584450.5:c.2396A>G
|
ENSP00000463714.1:p.Gln799Arg
|
|
|
ENST00000584601.5:c.2306A>G
|
ENSP00000462438.1:p.Gln769Arg
|
|
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NM_001005862.2:c.2306A>G , LRG_724t1:c.2306A>G
|
NP_001005862.1:p.Gln769Arg
|
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NM_001289936.1:c.2351A>G , LRG_724t4:c.2351A>G
|
NP_001276865.1:p.Gln784Arg
|
|
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NM_001289937.1:c.2396A>G
|
NP_001276866.1:p.Gln799Arg
|
|
|
NM_004448.3:c.2396A>G , LRG_724t2:c.2396A>G
|
NP_004439.2:p.Gln799Arg
|
|
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NR_110535.1:n.2720A>G
|
|
|
|
XM_024450641.1:c.2534A>G
|
XP_024306409.1:p.Gln845Arg
|
|
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XM_024450642.1:c.2489A>G
|
XP_024306410.1:p.Gln830Arg
|
|
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XM_024450643.1:c.2444A>G
|
XP_024306411.1:p.Gln815Arg
|
|
|
NM_001005862.3:c.2306A>G
|
NP_001005862.1:p.Gln769Arg
|
|
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NM_001289936.2:c.2351A>G
|
NP_001276865.1:p.Gln784Arg
|
|
|
NM_001289937.2:c.2396A>G
|
NP_001276866.1:p.Gln799Arg
|
|
|
NM_001382782.1:c.2306A>G
|
NP_001369711.1:p.Gln769Arg
|
|
|
NM_001382783.1:c.2306A>G
|
NP_001369712.1:p.Gln769Arg
|
|
|
NM_001382784.1:c.2513A>G
|
NP_001369713.1:p.Gln838Arg
|
|
|
NM_001382785.1:c.2498A>G
|
NP_001369714.1:p.Gln833Arg
|
|
|
NM_001382786.1:c.2477A>G
|
NP_001369715.1:p.Gln826Arg
|
|
|
NM_001382787.1:c.2471A>G
|
NP_001369716.1:p.Gln824Arg
|
|
|
NM_001382788.1:c.2426A>G
|
NP_001369717.1:p.Gln809Arg
|
|
|
NM_001382789.1:c.2417A>G
|
NP_001369718.1:p.Gln806Arg
|
|
|
NM_001382790.1:c.2393A>G
|
NP_001369719.1:p.Gln798Arg
|
|
|
NM_001382791.1:c.2387A>G
|
NP_001369720.1:p.Gln796Arg
|
|
|
NM_001382792.1:c.2360A>G
|
NP_001369721.1:p.Gln787Arg
|
|
|
NM_001382793.1:c.2354A>G
|
NP_001369722.1:p.Gln785Arg
|
|
|
NM_001382794.1:c.2354A>G
|
NP_001369723.1:p.Gln785Arg
|
|
|
NM_001382795.1:c.2348A>G
|
NP_001369724.1:p.Gln783Arg
|
|
|
NM_001382796.1:c.2396A>G
|
NP_001369725.1:p.Gln799Arg
|
|
|
NM_001382797.1:c.2297A>G
|
NP_001369726.1:p.Gln766Arg
|
|
|
NM_001382798.1:c.2396A>G
|
NP_001369727.1:p.Gln799Arg
|
|
|
NM_001382799.1:c.2216A>G
|
NP_001369728.1:p.Gln739Arg
|
|
|
NM_001382800.1:c.2308-235A>G
|
NP_001369729.1:n.2308-235A>G
|
|
|
NM_001382801.1:c.2348A>G
|
NP_001369730.1:p.Gln783Arg
|
|
|
NM_001382802.1:c.2138A>G
|
NP_001369731.1:p.Gln713Arg
|
|
|
NM_001382803.1:c.2354A>G
|
NP_001369732.1:p.Gln785Arg
|
|
|
NM_001382804.1:c.1568A>G
|
NP_001369733.1:p.Gln523Arg
|
|
|
NM_001382805.1:c.2208+1154A>G
|
NP_001369734.1:n.2208+1154A>G
|
|
|
NM_001382806.1:c.1358A>G
|
NP_001369735.1:p.Gln453Arg
|
|
|
NM_004448.4:c.2396A>G
MANE Select
|
NP_004439.2:p.Gln799Arg
|
|
|
NR_110535.2:n.2634A>G
|
|
|
