ENST00000269571.10:c.2520G>T
MANE Select
|
ENSP00000269571.4:p.Arg840=
|
|
ENST00000269571.9:c.2520G>T
|
ENSP00000269571.4:p.Arg840=
|
|
ENST00000406381.6:c.2430G>T
|
ENSP00000385185.2:p.Arg810=
|
|
ENST00000445658.6:c.1692G>T
|
ENSP00000404047.2:p.Arg564=
|
|
ENST00000541774.5:c.2475G>T
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ENSP00000446466.1:p.Arg825=
|
|
ENST00000578373.5:c.*2310G>T
|
ENSP00000463427.1:n.*2310G>T
|
|
ENST00000580074.1:c.626G>T
|
|
|
ENST00000583038.5:n.3654G>T
|
|
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ENST00000584450.5:c.2520G>T
|
ENSP00000463714.1:p.Arg840=
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|
ENST00000584601.5:c.2430G>T
|
ENSP00000462438.1:p.Arg810=
|
|
NM_001005862.2:c.2430G>T , LRG_724t1:c.2430G>T
|
NP_001005862.1:p.Arg810=
|
|
NM_001289936.1:c.2475G>T , LRG_724t4:c.2475G>T
|
NP_001276865.1:p.Arg825=
|
|
NM_001289937.1:c.2520G>T
|
NP_001276866.1:p.Arg840=
|
|
NM_004448.3:c.2520G>T , LRG_724t2:c.2520G>T
|
NP_004439.2:p.Arg840=
|
|
NR_110535.1:n.2844G>T
|
|
|
XM_024450641.1:c.2658G>T
|
XP_024306409.1:p.Arg886=
|
|
XM_024450642.1:c.2613G>T
|
XP_024306410.1:p.Arg871=
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|
XM_024450643.1:c.2568G>T
|
XP_024306411.1:p.Arg856=
|
|
NM_001005862.3:c.2430G>T
|
NP_001005862.1:p.Arg810=
|
|
NM_001289936.2:c.2475G>T
|
NP_001276865.1:p.Arg825=
|
|
NM_001289937.2:c.2520G>T
|
NP_001276866.1:p.Arg840=
|
|
NM_001382782.1:c.2430G>T
|
NP_001369711.1:p.Arg810=
|
|
NM_001382783.1:c.2430G>T
|
NP_001369712.1:p.Arg810=
|
|
NM_001382784.1:c.2637G>T
|
NP_001369713.1:p.Arg879=
|
|
NM_001382785.1:c.2622G>T
|
NP_001369714.1:p.Arg874=
|
|
NM_001382786.1:c.2601G>T
|
NP_001369715.1:p.Arg867=
|
|
NM_001382787.1:c.2595G>T
|
NP_001369716.1:p.Arg865=
|
|
NM_001382788.1:c.2550G>T
|
NP_001369717.1:p.Arg850=
|
|
NM_001382789.1:c.2541G>T
|
NP_001369718.1:p.Arg847=
|
|
NM_001382790.1:c.2517G>T
|
NP_001369719.1:p.Arg839=
|
|
NM_001382791.1:c.2511G>T
|
NP_001369720.1:p.Arg837=
|
|
NM_001382792.1:c.2484G>T
|
NP_001369721.1:p.Arg828=
|
|
NM_001382793.1:c.2478G>T
|
NP_001369722.1:p.Arg826=
|
|
NM_001382794.1:c.2478G>T
|
NP_001369723.1:p.Arg826=
|
|
NM_001382795.1:c.2472G>T
|
NP_001369724.1:p.Arg824=
|
|
NM_001382796.1:c.2520G>T
|
NP_001369725.1:p.Arg840=
|
|
NM_001382797.1:c.2421G>T
|
NP_001369726.1:p.Arg807=
|
|
NM_001382798.1:c.2493+164G>T
|
NP_001369727.1:n.2493+164G>T
|
|
NM_001382799.1:c.2340G>T
|
NP_001369728.1:p.Arg780=
|
|
NM_001382800.1:c.2334G>T
|
NP_001369729.1:p.Arg778=
|
|
NM_001382801.1:c.2445+164G>T
|
NP_001369730.1:n.2445+164G>T
|
|
NM_001382802.1:c.2262G>T
|
NP_001369731.1:p.Arg754=
|
|
NM_001382803.1:c.2478G>T
|
NP_001369732.1:p.Arg826=
|
|
NM_001382804.1:c.1692G>T
|
NP_001369733.1:p.Arg564=
|
|
NM_001382805.1:c.2208+1415G>T
|
NP_001369734.1:n.2208+1415G>T
|
|
NM_001382806.1:c.1482G>T
|
NP_001369735.1:p.Arg494=
|
|
NM_004448.4:c.2520G>T
MANE Select
|
NP_004439.2:p.Arg840=
|
|
NR_110535.2:n.2758G>T
|
|
|