ENST00000269571.10:c.3520T>A
MANE Select
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ENSP00000269571.4:p.Ser1174Thr
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ENST00000269571.9:c.3520T>A
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ENSP00000269571.4:p.Ser1174Thr
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ENST00000406381.6:c.3430T>A
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ENSP00000385185.2:p.Ser1144Thr
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ENST00000445658.6:c.2692T>A
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ENSP00000404047.2:p.Ser898Thr
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ENST00000541774.5:c.3475T>A
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ENSP00000446466.1:p.Ser1159Thr
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ENST00000578373.5:c.*3310T>A
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ENSP00000463427.1:n.*3310T>A
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ENST00000584450.5:c.*99T>A
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ENSP00000463714.1:n.*99T>A
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ENST00000584601.5:c.3430T>A
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ENSP00000462438.1:p.Ser1144Thr
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NM_001005862.2:c.3430T>A , LRG_724t1:c.3430T>A
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NP_001005862.1:p.Ser1144Thr
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NM_001289936.1:c.3475T>A , LRG_724t4:c.3475T>A
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NP_001276865.1:p.Ser1159Thr
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NM_001289937.1:c.*99T>A
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NP_001276866.1:n.*99T>A
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NM_004448.3:c.3520T>A , LRG_724t2:c.3520T>A
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NP_004439.2:p.Ser1174Thr
|
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NR_110535.1:n.3844T>A
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|
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XM_024450641.1:c.3658T>A
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XP_024306409.1:p.Ser1220Thr
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XM_024450642.1:c.3613T>A
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XP_024306410.1:p.Ser1205Thr
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XM_024450643.1:c.3568T>A
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XP_024306411.1:p.Ser1190Thr
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NM_001005862.3:c.3430T>A
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NP_001005862.1:p.Ser1144Thr
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NM_001289936.2:c.3475T>A
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NP_001276865.1:p.Ser1159Thr
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NM_001289937.2:c.*99T>A
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NP_001276866.1:n.*99T>A
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NM_001382782.1:c.3430T>A
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NP_001369711.1:p.Ser1144Thr
|
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NM_001382783.1:c.3430T>A
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NP_001369712.1:p.Ser1144Thr
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NM_001382784.1:c.3637T>A
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NP_001369713.1:p.Ser1213Thr
|
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NM_001382785.1:c.3622T>A
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NP_001369714.1:p.Ser1208Thr
|
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NM_001382786.1:c.3601T>A
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NP_001369715.1:p.Ser1201Thr
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NM_001382787.1:c.3595T>A
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NP_001369716.1:p.Ser1199Thr
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NM_001382788.1:c.3550T>A
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NP_001369717.1:p.Ser1184Thr
|
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NM_001382789.1:c.3541T>A
|
NP_001369718.1:p.Ser1181Thr
|
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NM_001382790.1:c.3517T>A
|
NP_001369719.1:p.Ser1173Thr
|
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NM_001382791.1:c.3511T>A
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NP_001369720.1:p.Ser1171Thr
|
|
NM_001382792.1:c.3484T>A
|
NP_001369721.1:p.Ser1162Thr
|
|
NM_001382793.1:c.3478T>A
|
NP_001369722.1:p.Ser1160Thr
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NM_001382794.1:c.3478T>A
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NP_001369723.1:p.Ser1160Thr
|
|
NM_001382795.1:c.3472T>A
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NP_001369724.1:p.Ser1158Thr
|
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NM_001382796.1:c.3433T>A
|
NP_001369725.1:p.Ser1145Thr
|
|
NM_001382797.1:c.3421T>A
|
NP_001369726.1:p.Ser1141Thr
|
|
NM_001382798.1:c.3364T>A
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NP_001369727.1:p.Ser1122Thr
|
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NM_001382799.1:c.3340T>A
|
NP_001369728.1:p.Ser1114Thr
|
|
NM_001382800.1:c.3334T>A
|
NP_001369729.1:p.Ser1112Thr
|
|
NM_001382801.1:c.3316T>A
|
NP_001369730.1:p.Ser1106Thr
|
|
NM_001382802.1:c.3262T>A
|
NP_001369731.1:p.Ser1088Thr
|
|
NM_001382803.1:c.*99T>A
|
NP_001369732.1:n.*99T>A
|
|
NM_001382804.1:c.2692T>A
|
NP_001369733.1:p.Ser898Thr
|
|
NM_001382805.1:c.2569T>A
|
NP_001369734.1:p.Ser857Thr
|
|
NM_001382806.1:c.2482T>A
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NP_001369735.1:p.Ser828Thr
|
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NM_004448.4:c.3520T>A
MANE Select
|
NP_004439.2:p.Ser1174Thr
|
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NR_110535.2:n.3758T>A
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|
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