ENST00000269571.10:c.2553G>T
MANE Select
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ENSP00000269571.4:p.Val851=
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ENST00000269571.9:c.2553G>T
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ENSP00000269571.4:p.Val851=
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ENST00000406381.6:c.2463G>T
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ENSP00000385185.2:p.Val821=
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ENST00000445658.6:c.1725G>T
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ENSP00000404047.2:p.Val575=
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ENST00000541774.5:c.2508G>T
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ENSP00000446466.1:p.Val836=
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ENST00000578373.5:c.*2343G>T
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ENSP00000463427.1:n.*2343G>T
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ENST00000580074.1:c.659G>T
|
|
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ENST00000583038.5:n.3687G>T
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ENST00000584450.5:c.2553G>T
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ENSP00000463714.1:p.Val851=
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ENST00000584601.5:c.2463G>T
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ENSP00000462438.1:p.Val821=
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NM_001005862.2:c.2463G>T , LRG_724t1:c.2463G>T
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NP_001005862.1:p.Val821=
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NM_001289936.1:c.2508G>T , LRG_724t4:c.2508G>T
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NP_001276865.1:p.Val836=
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NM_001289937.1:c.2553G>T
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NP_001276866.1:p.Val851=
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NM_004448.3:c.2553G>T , LRG_724t2:c.2553G>T
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NP_004439.2:p.Val851=
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NR_110535.1:n.2877G>T
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|
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XM_024450641.1:c.2691G>T
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XP_024306409.1:p.Val897=
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XM_024450642.1:c.2646G>T
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XP_024306410.1:p.Val882=
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XM_024450643.1:c.2601G>T
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XP_024306411.1:p.Val867=
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NM_001005862.3:c.2463G>T
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NP_001005862.1:p.Val821=
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NM_001289936.2:c.2508G>T
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NP_001276865.1:p.Val836=
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NM_001289937.2:c.2553G>T
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NP_001276866.1:p.Val851=
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NM_001382782.1:c.2463G>T
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NP_001369711.1:p.Val821=
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NM_001382783.1:c.2463G>T
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NP_001369712.1:p.Val821=
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|
NM_001382784.1:c.2670G>T
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NP_001369713.1:p.Val890=
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NM_001382785.1:c.2655G>T
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NP_001369714.1:p.Val885=
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NM_001382786.1:c.2634G>T
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NP_001369715.1:p.Val878=
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NM_001382787.1:c.2628G>T
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NP_001369716.1:p.Val876=
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|
NM_001382788.1:c.2583G>T
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NP_001369717.1:p.Val861=
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NM_001382789.1:c.2574G>T
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NP_001369718.1:p.Val858=
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NM_001382790.1:c.2550G>T
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NP_001369719.1:p.Val850=
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NM_001382791.1:c.2544G>T
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NP_001369720.1:p.Val848=
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|
NM_001382792.1:c.2517G>T
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NP_001369721.1:p.Val839=
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NM_001382793.1:c.2511G>T
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NP_001369722.1:p.Val837=
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|
NM_001382794.1:c.2511G>T
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NP_001369723.1:p.Val837=
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NM_001382795.1:c.2505G>T
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NP_001369724.1:p.Val835=
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NM_001382796.1:c.2553G>T
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NP_001369725.1:p.Val851=
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|
NM_001382797.1:c.2454G>T
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NP_001369726.1:p.Val818=
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|
NM_001382798.1:c.2493+197G>T
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NP_001369727.1:n.2493+197G>T
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|
NM_001382799.1:c.2373G>T
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NP_001369728.1:p.Val791=
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|
NM_001382800.1:c.2367G>T
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NP_001369729.1:p.Val789=
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|
NM_001382801.1:c.2445+197G>T
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NP_001369730.1:n.2445+197G>T
|
|
NM_001382802.1:c.2295G>T
|
NP_001369731.1:p.Val765=
|
|
NM_001382803.1:c.2511G>T
|
NP_001369732.1:p.Val837=
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|
NM_001382804.1:c.1725G>T
|
NP_001369733.1:p.Val575=
|
|
NM_001382805.1:c.2208+1448G>T
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NP_001369734.1:n.2208+1448G>T
|
|
NM_001382806.1:c.1515G>T
|
NP_001369735.1:p.Val505=
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|
NM_004448.4:c.2553G>T
MANE Select
|
NP_004439.2:p.Val851=
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|
NR_110535.2:n.2791G>T
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