ENST00000269571.10:c.2305G>C
MANE Select
|
ENSP00000269571.4:p.Asp769His
|
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ENST00000269571.9:c.2305G>C
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ENSP00000269571.4:p.Asp769His
|
|
ENST00000406381.6:c.2215G>C
|
ENSP00000385185.2:p.Asp739His
|
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ENST00000445658.6:c.1477G>C
|
ENSP00000404047.2:p.Asp493His
|
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ENST00000541774.5:c.2260G>C
|
ENSP00000446466.1:p.Asp754His
|
|
ENST00000578373.5:c.*2095G>C
|
ENSP00000463427.1:n.*2095G>C
|
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ENST00000580074.1:c.411G>C
|
|
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ENST00000583038.5:n.3439G>C
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|
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ENST00000584450.5:c.2305G>C
|
ENSP00000463714.1:p.Asp769His
|
|
ENST00000584601.5:c.2215G>C
|
ENSP00000462438.1:p.Asp739His
|
|
NM_001005862.2:c.2215G>C , LRG_724t1:c.2215G>C
|
NP_001005862.1:p.Asp739His
|
|
NM_001289936.1:c.2260G>C , LRG_724t4:c.2260G>C
|
NP_001276865.1:p.Asp754His
|
|
NM_001289937.1:c.2305G>C
|
NP_001276866.1:p.Asp769His
|
|
NM_004448.3:c.2305G>C , LRG_724t2:c.2305G>C
|
NP_004439.2:p.Asp769His
|
|
NR_110535.1:n.2629G>C
|
|
|
XM_024450641.1:c.2443G>C
|
XP_024306409.1:p.Asp815His
|
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XM_024450642.1:c.2398G>C
|
XP_024306410.1:p.Asp800His
|
|
XM_024450643.1:c.2353G>C
|
XP_024306411.1:p.Asp785His
|
|
NM_001005862.3:c.2215G>C
|
NP_001005862.1:p.Asp739His
|
|
NM_001289936.2:c.2260G>C
|
NP_001276865.1:p.Asp754His
|
|
NM_001289937.2:c.2305G>C
|
NP_001276866.1:p.Asp769His
|
|
NM_001382782.1:c.2215G>C
|
NP_001369711.1:p.Asp739His
|
|
NM_001382783.1:c.2215G>C
|
NP_001369712.1:p.Asp739His
|
|
NM_001382784.1:c.2422G>C
|
NP_001369713.1:p.Asp808His
|
|
NM_001382785.1:c.2407G>C
|
NP_001369714.1:p.Asp803His
|
|
NM_001382786.1:c.2386G>C
|
NP_001369715.1:p.Asp796His
|
|
NM_001382787.1:c.2380G>C
|
NP_001369716.1:p.Asp794His
|
|
NM_001382788.1:c.2335G>C
|
NP_001369717.1:p.Asp779His
|
|
NM_001382789.1:c.2326G>C
|
NP_001369718.1:p.Asp776His
|
|
NM_001382790.1:c.2302G>C
|
NP_001369719.1:p.Asp768His
|
|
NM_001382791.1:c.2296G>C
|
NP_001369720.1:p.Asp766His
|
|
NM_001382792.1:c.2269G>C
|
NP_001369721.1:p.Asp757His
|
|
NM_001382793.1:c.2263G>C
|
NP_001369722.1:p.Asp755His
|
|
NM_001382794.1:c.2263G>C
|
NP_001369723.1:p.Asp755His
|
|
NM_001382795.1:c.2257G>C
|
NP_001369724.1:p.Asp753His
|
|
NM_001382796.1:c.2305G>C
|
NP_001369725.1:p.Asp769His
|
|
NM_001382797.1:c.2208+348G>C
|
NP_001369726.1:n.2208+348G>C
|
|
NM_001382798.1:c.2305G>C
|
NP_001369727.1:p.Asp769His
|
|
NM_001382799.1:c.2125G>C
|
NP_001369728.1:p.Asp709His
|
|
NM_001382800.1:c.2305G>C
|
NP_001369729.1:p.Asp769His
|
|
NM_001382801.1:c.2257G>C
|
NP_001369730.1:p.Asp753His
|
|
NM_001382802.1:c.2047G>C
|
NP_001369731.1:p.Asp683His
|
|
NM_001382803.1:c.2263G>C
|
NP_001369732.1:p.Asp755His
|
|
NM_001382804.1:c.1477G>C
|
NP_001369733.1:p.Asp493His
|
|
NM_001382805.1:c.2208+348G>C
|
NP_001369734.1:n.2208+348G>C
|
|
NM_001382806.1:c.1267G>C
|
NP_001369735.1:p.Asp423His
|
|
NM_004448.4:c.2305G>C
MANE Select
|
NP_004439.2:p.Asp769His
|
|
NR_110535.2:n.2543G>C
|
|
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