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ENST00000269571.10:c.2528A>G
MANE Select
|
ENSP00000269571.4:p.His843Arg
|
|
|
ENST00000269571.9:c.2528A>G
|
ENSP00000269571.4:p.His843Arg
|
|
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ENST00000406381.6:c.2438A>G
|
ENSP00000385185.2:p.His813Arg
|
|
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ENST00000445658.6:c.1700A>G
|
ENSP00000404047.2:p.His567Arg
|
|
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ENST00000541774.5:c.2483A>G
|
ENSP00000446466.1:p.His828Arg
|
|
|
ENST00000578373.5:c.*2318A>G
|
ENSP00000463427.1:n.*2318A>G
|
|
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ENST00000580074.1:c.634A>G
|
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ENST00000583038.5:n.3662A>G
|
|
|
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ENST00000584450.5:c.2528A>G
|
ENSP00000463714.1:p.His843Arg
|
|
|
ENST00000584601.5:c.2438A>G
|
ENSP00000462438.1:p.His813Arg
|
|
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NM_001005862.2:c.2438A>G , LRG_724t1:c.2438A>G
|
NP_001005862.1:p.His813Arg
|
|
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NM_001289936.1:c.2483A>G , LRG_724t4:c.2483A>G
|
NP_001276865.1:p.His828Arg
|
|
|
NM_001289937.1:c.2528A>G
|
NP_001276866.1:p.His843Arg
|
|
|
NM_004448.3:c.2528A>G , LRG_724t2:c.2528A>G
|
NP_004439.2:p.His843Arg
|
|
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NR_110535.1:n.2852A>G
|
|
|
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XM_024450641.1:c.2666A>G
|
XP_024306409.1:p.His889Arg
|
|
|
XM_024450642.1:c.2621A>G
|
XP_024306410.1:p.His874Arg
|
|
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XM_024450643.1:c.2576A>G
|
XP_024306411.1:p.His859Arg
|
|
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NM_001005862.3:c.2438A>G
|
NP_001005862.1:p.His813Arg
|
|
|
NM_001289936.2:c.2483A>G
|
NP_001276865.1:p.His828Arg
|
|
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NM_001289937.2:c.2528A>G
|
NP_001276866.1:p.His843Arg
|
|
|
NM_001382782.1:c.2438A>G
|
NP_001369711.1:p.His813Arg
|
|
|
NM_001382783.1:c.2438A>G
|
NP_001369712.1:p.His813Arg
|
|
|
NM_001382784.1:c.2645A>G
|
NP_001369713.1:p.His882Arg
|
|
|
NM_001382785.1:c.2630A>G
|
NP_001369714.1:p.His877Arg
|
|
|
NM_001382786.1:c.2609A>G
|
NP_001369715.1:p.His870Arg
|
|
|
NM_001382787.1:c.2603A>G
|
NP_001369716.1:p.His868Arg
|
|
|
NM_001382788.1:c.2558A>G
|
NP_001369717.1:p.His853Arg
|
|
|
NM_001382789.1:c.2549A>G
|
NP_001369718.1:p.His850Arg
|
|
|
NM_001382790.1:c.2525A>G
|
NP_001369719.1:p.His842Arg
|
|
|
NM_001382791.1:c.2519A>G
|
NP_001369720.1:p.His840Arg
|
|
|
NM_001382792.1:c.2492A>G
|
NP_001369721.1:p.His831Arg
|
|
|
NM_001382793.1:c.2486A>G
|
NP_001369722.1:p.His829Arg
|
|
|
NM_001382794.1:c.2486A>G
|
NP_001369723.1:p.His829Arg
|
|
|
NM_001382795.1:c.2480A>G
|
NP_001369724.1:p.His827Arg
|
|
|
NM_001382796.1:c.2528A>G
|
NP_001369725.1:p.His843Arg
|
|
|
NM_001382797.1:c.2429A>G
|
NP_001369726.1:p.His810Arg
|
|
|
NM_001382798.1:c.2493+172A>G
|
NP_001369727.1:n.2493+172A>G
|
|
|
NM_001382799.1:c.2348A>G
|
NP_001369728.1:p.His783Arg
|
|
|
NM_001382800.1:c.2342A>G
|
NP_001369729.1:p.His781Arg
|
|
|
NM_001382801.1:c.2445+172A>G
|
NP_001369730.1:n.2445+172A>G
|
|
|
NM_001382802.1:c.2270A>G
|
NP_001369731.1:p.His757Arg
|
|
|
NM_001382803.1:c.2486A>G
|
NP_001369732.1:p.His829Arg
|
|
|
NM_001382804.1:c.1700A>G
|
NP_001369733.1:p.His567Arg
|
|
|
NM_001382805.1:c.2208+1423A>G
|
NP_001369734.1:n.2208+1423A>G
|
|
|
NM_001382806.1:c.1490A>G
|
NP_001369735.1:p.His497Arg
|
|
|
NM_004448.4:c.2528A>G
MANE Select
|
NP_004439.2:p.His843Arg
|
|
|
NR_110535.2:n.2766A>G
|
|
|
