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ENST00000269571.10:c.2335T>G
MANE Select
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ENSP00000269571.4:p.Ser779Ala
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ENST00000269571.9:c.2335T>G
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ENSP00000269571.4:p.Ser779Ala
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ENST00000406381.6:c.2245T>G
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ENSP00000385185.2:p.Ser749Ala
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ENST00000445658.6:c.1507T>G
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ENSP00000404047.2:p.Ser503Ala
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ENST00000541774.5:c.2290T>G
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ENSP00000446466.1:p.Ser764Ala
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ENST00000578373.5:c.*2125T>G
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ENSP00000463427.1:n.*2125T>G
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ENST00000580074.1:c.441T>G
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ENST00000583038.5:n.3469T>G
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ENST00000584450.5:c.2335T>G
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ENSP00000463714.1:p.Ser779Ala
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ENST00000584601.5:c.2245T>G
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ENSP00000462438.1:p.Ser749Ala
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NM_001005862.2:c.2245T>G , LRG_724t1:c.2245T>G
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NP_001005862.1:p.Ser749Ala
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NM_001289936.1:c.2290T>G , LRG_724t4:c.2290T>G
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NP_001276865.1:p.Ser764Ala
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NM_001289937.1:c.2335T>G
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NP_001276866.1:p.Ser779Ala
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NM_004448.3:c.2335T>G , LRG_724t2:c.2335T>G
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NP_004439.2:p.Ser779Ala
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NR_110535.1:n.2659T>G
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XM_024450641.1:c.2473T>G
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XP_024306409.1:p.Ser825Ala
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XM_024450642.1:c.2428T>G
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XP_024306410.1:p.Ser810Ala
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XM_024450643.1:c.2383T>G
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XP_024306411.1:p.Ser795Ala
|
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NM_001005862.3:c.2245T>G
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NP_001005862.1:p.Ser749Ala
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NM_001289936.2:c.2290T>G
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NP_001276865.1:p.Ser764Ala
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NM_001289937.2:c.2335T>G
|
NP_001276866.1:p.Ser779Ala
|
|
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NM_001382782.1:c.2245T>G
|
NP_001369711.1:p.Ser749Ala
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NM_001382783.1:c.2245T>G
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NP_001369712.1:p.Ser749Ala
|
|
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NM_001382784.1:c.2452T>G
|
NP_001369713.1:p.Ser818Ala
|
|
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NM_001382785.1:c.2437T>G
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NP_001369714.1:p.Ser813Ala
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NM_001382786.1:c.2416T>G
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NP_001369715.1:p.Ser806Ala
|
|
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NM_001382787.1:c.2410T>G
|
NP_001369716.1:p.Ser804Ala
|
|
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NM_001382788.1:c.2365T>G
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NP_001369717.1:p.Ser789Ala
|
|
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NM_001382789.1:c.2356T>G
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NP_001369718.1:p.Ser786Ala
|
|
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NM_001382790.1:c.2332T>G
|
NP_001369719.1:p.Ser778Ala
|
|
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NM_001382791.1:c.2326T>G
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NP_001369720.1:p.Ser776Ala
|
|
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NM_001382792.1:c.2299T>G
|
NP_001369721.1:p.Ser767Ala
|
|
|
NM_001382793.1:c.2293T>G
|
NP_001369722.1:p.Ser765Ala
|
|
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NM_001382794.1:c.2293T>G
|
NP_001369723.1:p.Ser765Ala
|
|
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NM_001382795.1:c.2287T>G
|
NP_001369724.1:p.Ser763Ala
|
|
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NM_001382796.1:c.2335T>G
|
NP_001369725.1:p.Ser779Ala
|
|
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NM_001382797.1:c.2236T>G
|
NP_001369726.1:p.Ser746Ala
|
|
|
NM_001382798.1:c.2335T>G
|
NP_001369727.1:p.Ser779Ala
|
|
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NM_001382799.1:c.2155T>G
|
NP_001369728.1:p.Ser719Ala
|
|
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NM_001382800.1:c.2308-296T>G
|
NP_001369729.1:n.2308-296T>G
|
|
|
NM_001382801.1:c.2287T>G
|
NP_001369730.1:p.Ser763Ala
|
|
|
NM_001382802.1:c.2077T>G
|
NP_001369731.1:p.Ser693Ala
|
|
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NM_001382803.1:c.2293T>G
|
NP_001369732.1:p.Ser765Ala
|
|
|
NM_001382804.1:c.1507T>G
|
NP_001369733.1:p.Ser503Ala
|
|
|
NM_001382805.1:c.2208+1093T>G
|
NP_001369734.1:n.2208+1093T>G
|
|
|
NM_001382806.1:c.1297T>G
|
NP_001369735.1:p.Ser433Ala
|
|
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NM_004448.4:c.2335T>G
MANE Select
|
NP_004439.2:p.Ser779Ala
|
|
|
NR_110535.2:n.2573T>G
|
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