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ENST00000269571.10:c.3257T>G
MANE Select
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ENSP00000269571.4:p.Phe1086Cys
|
|
|
ENST00000269571.9:c.3257T>G
|
ENSP00000269571.4:p.Phe1086Cys
|
|
|
ENST00000406381.6:c.3167T>G
|
ENSP00000385185.2:p.Phe1056Cys
|
|
|
ENST00000445658.6:c.2429T>G
|
ENSP00000404047.2:p.Phe810Cys
|
|
|
ENST00000541774.5:c.3212T>G
|
ENSP00000446466.1:p.Phe1071Cys
|
|
|
ENST00000578373.5:c.*3047T>G
|
ENSP00000463427.1:n.*3047T>G
|
|
|
ENST00000584450.5:c.3160-297T>G
|
ENSP00000463714.1:n.3160-297T>G
|
|
|
ENST00000584601.5:c.3167T>G
|
ENSP00000462438.1:p.Phe1056Cys
|
|
|
NM_001005862.2:c.3167T>G , LRG_724t1:c.3167T>G
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NP_001005862.1:p.Phe1056Cys
|
|
|
NM_001289936.1:c.3212T>G , LRG_724t4:c.3212T>G
|
NP_001276865.1:p.Phe1071Cys
|
|
|
NM_001289937.1:c.3160-297T>G
|
NP_001276866.1:n.3160-297T>G
|
|
|
NM_004448.3:c.3257T>G , LRG_724t2:c.3257T>G
|
NP_004439.2:p.Phe1086Cys
|
|
|
NR_110535.1:n.3581T>G
|
|
|
|
XM_024450641.1:c.3395T>G
|
XP_024306409.1:p.Phe1132Cys
|
|
|
XM_024450642.1:c.3350T>G
|
XP_024306410.1:p.Phe1117Cys
|
|
|
XM_024450643.1:c.3305T>G
|
XP_024306411.1:p.Phe1102Cys
|
|
|
NM_001005862.3:c.3167T>G
|
NP_001005862.1:p.Phe1056Cys
|
|
|
NM_001289936.2:c.3212T>G
|
NP_001276865.1:p.Phe1071Cys
|
|
|
NM_001289937.2:c.3160-297T>G
|
NP_001276866.1:n.3160-297T>G
|
|
|
NM_001382782.1:c.3167T>G
|
NP_001369711.1:p.Phe1056Cys
|
|
|
NM_001382783.1:c.3167T>G
|
NP_001369712.1:p.Phe1056Cys
|
|
|
NM_001382784.1:c.3374T>G
|
NP_001369713.1:p.Phe1125Cys
|
|
|
NM_001382785.1:c.3359T>G
|
NP_001369714.1:p.Phe1120Cys
|
|
|
NM_001382786.1:c.3338T>G
|
NP_001369715.1:p.Phe1113Cys
|
|
|
NM_001382787.1:c.3332T>G
|
NP_001369716.1:p.Phe1111Cys
|
|
|
NM_001382788.1:c.3287T>G
|
NP_001369717.1:p.Phe1096Cys
|
|
|
NM_001382789.1:c.3278T>G
|
NP_001369718.1:p.Phe1093Cys
|
|
|
NM_001382790.1:c.3254T>G
|
NP_001369719.1:p.Phe1085Cys
|
|
|
NM_001382791.1:c.3248T>G
|
NP_001369720.1:p.Phe1083Cys
|
|
|
NM_001382792.1:c.3221T>G
|
NP_001369721.1:p.Phe1074Cys
|
|
|
NM_001382793.1:c.3215T>G
|
NP_001369722.1:p.Phe1072Cys
|
|
|
NM_001382794.1:c.3215T>G
|
NP_001369723.1:p.Phe1072Cys
|
|
|
NM_001382795.1:c.3209T>G
|
NP_001369724.1:p.Phe1070Cys
|
|
|
NM_001382796.1:c.3170T>G
|
NP_001369725.1:p.Phe1057Cys
|
|
|
NM_001382797.1:c.3158T>G
|
NP_001369726.1:p.Phe1053Cys
|
|
|
NM_001382798.1:c.3101T>G
|
NP_001369727.1:p.Phe1034Cys
|
|
|
NM_001382799.1:c.3077T>G
|
NP_001369728.1:p.Phe1026Cys
|
|
|
NM_001382800.1:c.3071T>G
|
NP_001369729.1:p.Phe1024Cys
|
|
|
NM_001382801.1:c.3053T>G
|
NP_001369730.1:p.Phe1018Cys
|
|
|
NM_001382802.1:c.2999T>G
|
NP_001369731.1:p.Phe1000Cys
|
|
|
NM_001382803.1:c.3118-297T>G
|
NP_001369732.1:n.3118-297T>G
|
|
|
NM_001382804.1:c.2429T>G
|
NP_001369733.1:p.Phe810Cys
|
|
|
NM_001382805.1:c.2306T>G
|
NP_001369734.1:p.Phe769Cys
|
|
|
NM_001382806.1:c.2219T>G
|
NP_001369735.1:p.Phe740Cys
|
|
|
NM_004448.4:c.3257T>G
MANE Select
|
NP_004439.2:p.Phe1086Cys
|
|
|
NR_110535.2:n.3495T>G
|
|
|
