ENST00000269571.10:c.3217T>A
MANE Select
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ENSP00000269571.4:p.Ser1073Thr
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ENST00000269571.9:c.3217T>A
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ENSP00000269571.4:p.Ser1073Thr
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ENST00000406381.6:c.3127T>A
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ENSP00000385185.2:p.Ser1043Thr
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ENST00000445658.6:c.2389T>A
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ENSP00000404047.2:p.Ser797Thr
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ENST00000541774.5:c.3172T>A
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ENSP00000446466.1:p.Ser1058Thr
|
|
ENST00000578373.5:c.*3007T>A
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ENSP00000463427.1:n.*3007T>A
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ENST00000584450.5:c.3160-337T>A
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ENSP00000463714.1:n.3160-337T>A
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ENST00000584601.5:c.3127T>A
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ENSP00000462438.1:p.Ser1043Thr
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NM_001005862.2:c.3127T>A , LRG_724t1:c.3127T>A
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NP_001005862.1:p.Ser1043Thr
|
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NM_001289936.1:c.3172T>A , LRG_724t4:c.3172T>A
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NP_001276865.1:p.Ser1058Thr
|
|
NM_001289937.1:c.3160-337T>A
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NP_001276866.1:n.3160-337T>A
|
|
NM_004448.3:c.3217T>A , LRG_724t2:c.3217T>A
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NP_004439.2:p.Ser1073Thr
|
|
NR_110535.1:n.3541T>A
|
|
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XM_024450641.1:c.3355T>A
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XP_024306409.1:p.Ser1119Thr
|
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XM_024450642.1:c.3310T>A
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XP_024306410.1:p.Ser1104Thr
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|
XM_024450643.1:c.3265T>A
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XP_024306411.1:p.Ser1089Thr
|
|
NM_001005862.3:c.3127T>A
|
NP_001005862.1:p.Ser1043Thr
|
|
NM_001289936.2:c.3172T>A
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NP_001276865.1:p.Ser1058Thr
|
|
NM_001289937.2:c.3160-337T>A
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NP_001276866.1:n.3160-337T>A
|
|
NM_001382782.1:c.3127T>A
|
NP_001369711.1:p.Ser1043Thr
|
|
NM_001382783.1:c.3127T>A
|
NP_001369712.1:p.Ser1043Thr
|
|
NM_001382784.1:c.3334T>A
|
NP_001369713.1:p.Ser1112Thr
|
|
NM_001382785.1:c.3319T>A
|
NP_001369714.1:p.Ser1107Thr
|
|
NM_001382786.1:c.3298T>A
|
NP_001369715.1:p.Ser1100Thr
|
|
NM_001382787.1:c.3292T>A
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NP_001369716.1:p.Ser1098Thr
|
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NM_001382788.1:c.3247T>A
|
NP_001369717.1:p.Ser1083Thr
|
|
NM_001382789.1:c.3238T>A
|
NP_001369718.1:p.Ser1080Thr
|
|
NM_001382790.1:c.3214T>A
|
NP_001369719.1:p.Ser1072Thr
|
|
NM_001382791.1:c.3208T>A
|
NP_001369720.1:p.Ser1070Thr
|
|
NM_001382792.1:c.3181T>A
|
NP_001369721.1:p.Ser1061Thr
|
|
NM_001382793.1:c.3175T>A
|
NP_001369722.1:p.Ser1059Thr
|
|
NM_001382794.1:c.3175T>A
|
NP_001369723.1:p.Ser1059Thr
|
|
NM_001382795.1:c.3169T>A
|
NP_001369724.1:p.Ser1057Thr
|
|
NM_001382796.1:c.3130T>A
|
NP_001369725.1:p.Ser1044Thr
|
|
NM_001382797.1:c.3118T>A
|
NP_001369726.1:p.Ser1040Thr
|
|
NM_001382798.1:c.3061T>A
|
NP_001369727.1:p.Ser1021Thr
|
|
NM_001382799.1:c.3037T>A
|
NP_001369728.1:p.Ser1013Thr
|
|
NM_001382800.1:c.3031T>A
|
NP_001369729.1:p.Ser1011Thr
|
|
NM_001382801.1:c.3013T>A
|
NP_001369730.1:p.Ser1005Thr
|
|
NM_001382802.1:c.2959T>A
|
NP_001369731.1:p.Ser987Thr
|
|
NM_001382803.1:c.3118-337T>A
|
NP_001369732.1:n.3118-337T>A
|
|
NM_001382804.1:c.2389T>A
|
NP_001369733.1:p.Ser797Thr
|
|
NM_001382805.1:c.2266T>A
|
NP_001369734.1:p.Ser756Thr
|
|
NM_001382806.1:c.2179T>A
|
NP_001369735.1:p.Ser727Thr
|
|
NM_004448.4:c.3217T>A
MANE Select
|
NP_004439.2:p.Ser1073Thr
|
|
NR_110535.2:n.3455T>A
|
|
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