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ENST00000269571.10:c.2548A>G
MANE Select
|
ENSP00000269571.4:p.Asn850Asp
|
|
|
ENST00000269571.9:c.2548A>G
|
ENSP00000269571.4:p.Asn850Asp
|
|
|
ENST00000406381.6:c.2458A>G
|
ENSP00000385185.2:p.Asn820Asp
|
|
|
ENST00000445658.6:c.1720A>G
|
ENSP00000404047.2:p.Asn574Asp
|
|
|
ENST00000541774.5:c.2503A>G
|
ENSP00000446466.1:p.Asn835Asp
|
|
|
ENST00000578373.5:c.*2338A>G
|
ENSP00000463427.1:n.*2338A>G
|
|
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ENST00000580074.1:c.654A>G
|
|
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ENST00000583038.5:n.3682A>G
|
|
|
|
ENST00000584450.5:c.2548A>G
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ENSP00000463714.1:p.Asn850Asp
|
|
|
ENST00000584601.5:c.2458A>G
|
ENSP00000462438.1:p.Asn820Asp
|
|
|
NM_001005862.2:c.2458A>G , LRG_724t1:c.2458A>G
|
NP_001005862.1:p.Asn820Asp
|
|
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NM_001289936.1:c.2503A>G , LRG_724t4:c.2503A>G
|
NP_001276865.1:p.Asn835Asp
|
|
|
NM_001289937.1:c.2548A>G
|
NP_001276866.1:p.Asn850Asp
|
|
|
NM_004448.3:c.2548A>G , LRG_724t2:c.2548A>G
|
NP_004439.2:p.Asn850Asp
|
|
|
NR_110535.1:n.2872A>G
|
|
|
|
XM_024450641.1:c.2686A>G
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XP_024306409.1:p.Asn896Asp
|
|
|
XM_024450642.1:c.2641A>G
|
XP_024306410.1:p.Asn881Asp
|
|
|
XM_024450643.1:c.2596A>G
|
XP_024306411.1:p.Asn866Asp
|
|
|
NM_001005862.3:c.2458A>G
|
NP_001005862.1:p.Asn820Asp
|
|
|
NM_001289936.2:c.2503A>G
|
NP_001276865.1:p.Asn835Asp
|
|
|
NM_001289937.2:c.2548A>G
|
NP_001276866.1:p.Asn850Asp
|
|
|
NM_001382782.1:c.2458A>G
|
NP_001369711.1:p.Asn820Asp
|
|
|
NM_001382783.1:c.2458A>G
|
NP_001369712.1:p.Asn820Asp
|
|
|
NM_001382784.1:c.2665A>G
|
NP_001369713.1:p.Asn889Asp
|
|
|
NM_001382785.1:c.2650A>G
|
NP_001369714.1:p.Asn884Asp
|
|
|
NM_001382786.1:c.2629A>G
|
NP_001369715.1:p.Asn877Asp
|
|
|
NM_001382787.1:c.2623A>G
|
NP_001369716.1:p.Asn875Asp
|
|
|
NM_001382788.1:c.2578A>G
|
NP_001369717.1:p.Asn860Asp
|
|
|
NM_001382789.1:c.2569A>G
|
NP_001369718.1:p.Asn857Asp
|
|
|
NM_001382790.1:c.2545A>G
|
NP_001369719.1:p.Asn849Asp
|
|
|
NM_001382791.1:c.2539A>G
|
NP_001369720.1:p.Asn847Asp
|
|
|
NM_001382792.1:c.2512A>G
|
NP_001369721.1:p.Asn838Asp
|
|
|
NM_001382793.1:c.2506A>G
|
NP_001369722.1:p.Asn836Asp
|
|
|
NM_001382794.1:c.2506A>G
|
NP_001369723.1:p.Asn836Asp
|
|
|
NM_001382795.1:c.2500A>G
|
NP_001369724.1:p.Asn834Asp
|
|
|
NM_001382796.1:c.2548A>G
|
NP_001369725.1:p.Asn850Asp
|
|
|
NM_001382797.1:c.2449A>G
|
NP_001369726.1:p.Asn817Asp
|
|
|
NM_001382798.1:c.2493+192A>G
|
NP_001369727.1:n.2493+192A>G
|
|
|
NM_001382799.1:c.2368A>G
|
NP_001369728.1:p.Asn790Asp
|
|
|
NM_001382800.1:c.2362A>G
|
NP_001369729.1:p.Asn788Asp
|
|
|
NM_001382801.1:c.2445+192A>G
|
NP_001369730.1:n.2445+192A>G
|
|
|
NM_001382802.1:c.2290A>G
|
NP_001369731.1:p.Asn764Asp
|
|
|
NM_001382803.1:c.2506A>G
|
NP_001369732.1:p.Asn836Asp
|
|
|
NM_001382804.1:c.1720A>G
|
NP_001369733.1:p.Asn574Asp
|
|
|
NM_001382805.1:c.2208+1443A>G
|
NP_001369734.1:n.2208+1443A>G
|
|
|
NM_001382806.1:c.1510A>G
|
NP_001369735.1:p.Asn504Asp
|
|
|
NM_004448.4:c.2548A>G
MANE Select
|
NP_004439.2:p.Asn850Asp
|
|
|
NR_110535.2:n.2786A>G
|
|
|
