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ENST00000269571.10:c.2706G>T
MANE Select
|
ENSP00000269571.4:p.Gln902His
|
|
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ENST00000269571.9:c.2706G>T
|
ENSP00000269571.4:p.Gln902His
|
|
|
ENST00000406381.6:c.2616G>T
|
ENSP00000385185.2:p.Gln872His
|
|
|
ENST00000445658.6:c.1878G>T
|
ENSP00000404047.2:p.Gln626His
|
|
|
ENST00000541774.5:c.2661G>T
|
ENSP00000446466.1:p.Gln887His
|
|
|
ENST00000578373.5:c.*2496G>T
|
ENSP00000463427.1:n.*2496G>T
|
|
|
ENST00000583038.5:n.3962G>T
|
|
|
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ENST00000584450.5:c.2706G>T
|
ENSP00000463714.1:p.Gln902His
|
|
|
ENST00000584601.5:c.2616G>T
|
ENSP00000462438.1:p.Gln872His
|
|
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NM_001005862.2:c.2616G>T , LRG_724t1:c.2616G>T
|
NP_001005862.1:p.Gln872His
|
|
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NM_001289936.1:c.2661G>T , LRG_724t4:c.2661G>T
|
NP_001276865.1:p.Gln887His
|
|
|
NM_001289937.1:c.2706G>T
|
NP_001276866.1:p.Gln902His
|
|
|
NM_004448.3:c.2706G>T , LRG_724t2:c.2706G>T
|
NP_004439.2:p.Gln902His
|
|
|
NR_110535.1:n.3030G>T
|
|
|
|
XM_024450641.1:c.2844G>T
|
XP_024306409.1:p.Gln948His
|
|
|
XM_024450642.1:c.2799G>T
|
XP_024306410.1:p.Gln933His
|
|
|
XM_024450643.1:c.2754G>T
|
XP_024306411.1:p.Gln918His
|
|
|
NM_001005862.3:c.2616G>T
|
NP_001005862.1:p.Gln872His
|
|
|
NM_001289936.2:c.2661G>T
|
NP_001276865.1:p.Gln887His
|
|
|
NM_001289937.2:c.2706G>T
|
NP_001276866.1:p.Gln902His
|
|
|
NM_001382782.1:c.2616G>T
|
NP_001369711.1:p.Gln872His
|
|
|
NM_001382783.1:c.2616G>T
|
NP_001369712.1:p.Gln872His
|
|
|
NM_001382784.1:c.2823G>T
|
NP_001369713.1:p.Gln941His
|
|
|
NM_001382785.1:c.2808G>T
|
NP_001369714.1:p.Gln936His
|
|
|
NM_001382786.1:c.2787G>T
|
NP_001369715.1:p.Gln929His
|
|
|
NM_001382787.1:c.2781G>T
|
NP_001369716.1:p.Gln927His
|
|
|
NM_001382788.1:c.2736G>T
|
NP_001369717.1:p.Gln912His
|
|
|
NM_001382789.1:c.2727G>T
|
NP_001369718.1:p.Gln909His
|
|
|
NM_001382790.1:c.2703G>T
|
NP_001369719.1:p.Gln901His
|
|
|
NM_001382791.1:c.2697G>T
|
NP_001369720.1:p.Gln899His
|
|
|
NM_001382792.1:c.2670G>T
|
NP_001369721.1:p.Gln890His
|
|
|
NM_001382793.1:c.2664G>T
|
NP_001369722.1:p.Gln888His
|
|
|
NM_001382794.1:c.2664G>T
|
NP_001369723.1:p.Gln888His
|
|
|
NM_001382795.1:c.2658G>T
|
NP_001369724.1:p.Gln886His
|
|
|
NM_001382796.1:c.2706G>T
|
NP_001369725.1:p.Gln902His
|
|
|
NM_001382797.1:c.2607G>T
|
NP_001369726.1:p.Gln869His
|
|
|
NM_001382798.1:c.2550G>T
|
NP_001369727.1:p.Gln850His
|
|
|
NM_001382799.1:c.2526G>T
|
NP_001369728.1:p.Gln842His
|
|
|
NM_001382800.1:c.2520G>T
|
NP_001369729.1:p.Gln840His
|
|
|
NM_001382801.1:c.2502G>T
|
NP_001369730.1:p.Gln834His
|
|
|
NM_001382802.1:c.2448G>T
|
NP_001369731.1:p.Gln816His
|
|
|
NM_001382803.1:c.2664G>T
|
NP_001369732.1:p.Gln888His
|
|
|
NM_001382804.1:c.1878G>T
|
NP_001369733.1:p.Gln626His
|
|
|
NM_001382805.1:c.2208+1723G>T
|
NP_001369734.1:n.2208+1723G>T
|
|
|
NM_001382806.1:c.1668G>T
|
NP_001369735.1:p.Gln556His
|
|
|
NM_004448.4:c.2706G>T
MANE Select
|
NP_004439.2:p.Gln902His
|
|
|
NR_110535.2:n.2944G>T
|
|
|
