ENST00000269571.10:c.2394A>C
MANE Select
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ENSP00000269571.4:p.Thr798=
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ENST00000269571.9:c.2394A>C
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ENSP00000269571.4:p.Thr798=
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ENST00000406381.6:c.2304A>C
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ENSP00000385185.2:p.Thr768=
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ENST00000445658.6:c.1566A>C
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ENSP00000404047.2:p.Thr522=
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ENST00000541774.5:c.2349A>C
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ENSP00000446466.1:p.Thr783=
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ENST00000578373.5:c.*2184A>C
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ENSP00000463427.1:n.*2184A>C
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ENST00000580074.1:c.500A>C
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ENST00000583038.5:n.3528A>C
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ENST00000584450.5:c.2394A>C
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ENSP00000463714.1:p.Thr798=
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ENST00000584601.5:c.2304A>C
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ENSP00000462438.1:p.Thr768=
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NM_001005862.2:c.2304A>C , LRG_724t1:c.2304A>C
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NP_001005862.1:p.Thr768=
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NM_001289936.1:c.2349A>C , LRG_724t4:c.2349A>C
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NP_001276865.1:p.Thr783=
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NM_001289937.1:c.2394A>C
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NP_001276866.1:p.Thr798=
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NM_004448.3:c.2394A>C , LRG_724t2:c.2394A>C
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NP_004439.2:p.Thr798=
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NR_110535.1:n.2718A>C
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|
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XM_024450641.1:c.2532A>C
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XP_024306409.1:p.Thr844=
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XM_024450642.1:c.2487A>C
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XP_024306410.1:p.Thr829=
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XM_024450643.1:c.2442A>C
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XP_024306411.1:p.Thr814=
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NM_001005862.3:c.2304A>C
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NP_001005862.1:p.Thr768=
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NM_001289936.2:c.2349A>C
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NP_001276865.1:p.Thr783=
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NM_001289937.2:c.2394A>C
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NP_001276866.1:p.Thr798=
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NM_001382782.1:c.2304A>C
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NP_001369711.1:p.Thr768=
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NM_001382783.1:c.2304A>C
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NP_001369712.1:p.Thr768=
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NM_001382784.1:c.2511A>C
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NP_001369713.1:p.Thr837=
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NM_001382785.1:c.2496A>C
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NP_001369714.1:p.Thr832=
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NM_001382786.1:c.2475A>C
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NP_001369715.1:p.Thr825=
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NM_001382787.1:c.2469A>C
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NP_001369716.1:p.Thr823=
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NM_001382788.1:c.2424A>C
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NP_001369717.1:p.Thr808=
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NM_001382789.1:c.2415A>C
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NP_001369718.1:p.Thr805=
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NM_001382790.1:c.2391A>C
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NP_001369719.1:p.Thr797=
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NM_001382791.1:c.2385A>C
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NP_001369720.1:p.Thr795=
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NM_001382792.1:c.2358A>C
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NP_001369721.1:p.Thr786=
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NM_001382793.1:c.2352A>C
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NP_001369722.1:p.Thr784=
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NM_001382794.1:c.2352A>C
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NP_001369723.1:p.Thr784=
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NM_001382795.1:c.2346A>C
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NP_001369724.1:p.Thr782=
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NM_001382796.1:c.2394A>C
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NP_001369725.1:p.Thr798=
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NM_001382797.1:c.2295A>C
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NP_001369726.1:p.Thr765=
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NM_001382798.1:c.2394A>C
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NP_001369727.1:p.Thr798=
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NM_001382799.1:c.2214A>C
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NP_001369728.1:p.Thr738=
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NM_001382800.1:c.2308-237A>C
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NP_001369729.1:n.2308-237A>C
|
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NM_001382801.1:c.2346A>C
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NP_001369730.1:p.Thr782=
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NM_001382802.1:c.2136A>C
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NP_001369731.1:p.Thr712=
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NM_001382803.1:c.2352A>C
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NP_001369732.1:p.Thr784=
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NM_001382804.1:c.1566A>C
|
NP_001369733.1:p.Thr522=
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NM_001382805.1:c.2208+1152A>C
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NP_001369734.1:n.2208+1152A>C
|
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NM_001382806.1:c.1356A>C
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NP_001369735.1:p.Thr452=
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NM_004448.4:c.2394A>C
MANE Select
|
NP_004439.2:p.Thr798=
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NR_110535.2:n.2632A>C
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