ENST00000269571.10:c.3340G>T
MANE Select
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ENSP00000269571.4:p.Glu1114Ter
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ENST00000269571.9:c.3340G>T
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ENSP00000269571.4:p.Glu1114Ter
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ENST00000406381.6:c.3250G>T
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ENSP00000385185.2:p.Glu1084Ter
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ENST00000445658.6:c.2512G>T
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ENSP00000404047.2:p.Glu838Ter
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ENST00000541774.5:c.3295G>T
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ENSP00000446466.1:p.Glu1099Ter
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ENST00000578373.5:c.*3130G>T
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ENSP00000463427.1:n.*3130G>T
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ENST00000584450.5:c.3160-214G>T
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ENSP00000463714.1:n.3160-214G>T
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ENST00000584601.5:c.3250G>T
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ENSP00000462438.1:p.Glu1084Ter
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NM_001005862.2:c.3250G>T , LRG_724t1:c.3250G>T
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NP_001005862.1:p.Glu1084Ter
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NM_001289936.1:c.3295G>T , LRG_724t4:c.3295G>T
|
NP_001276865.1:p.Glu1099Ter
|
|
NM_001289937.1:c.3160-214G>T
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NP_001276866.1:n.3160-214G>T
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NM_004448.3:c.3340G>T , LRG_724t2:c.3340G>T
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NP_004439.2:p.Glu1114Ter
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NR_110535.1:n.3664G>T
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|
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XM_024450641.1:c.3478G>T
|
XP_024306409.1:p.Glu1160Ter
|
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XM_024450642.1:c.3433G>T
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XP_024306410.1:p.Glu1145Ter
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XM_024450643.1:c.3388G>T
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XP_024306411.1:p.Glu1130Ter
|
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NM_001005862.3:c.3250G>T
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NP_001005862.1:p.Glu1084Ter
|
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NM_001289936.2:c.3295G>T
|
NP_001276865.1:p.Glu1099Ter
|
|
NM_001289937.2:c.3160-214G>T
|
NP_001276866.1:n.3160-214G>T
|
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NM_001382782.1:c.3250G>T
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NP_001369711.1:p.Glu1084Ter
|
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NM_001382783.1:c.3250G>T
|
NP_001369712.1:p.Glu1084Ter
|
|
NM_001382784.1:c.3457G>T
|
NP_001369713.1:p.Glu1153Ter
|
|
NM_001382785.1:c.3442G>T
|
NP_001369714.1:p.Glu1148Ter
|
|
NM_001382786.1:c.3421G>T
|
NP_001369715.1:p.Glu1141Ter
|
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NM_001382787.1:c.3415G>T
|
NP_001369716.1:p.Glu1139Ter
|
|
NM_001382788.1:c.3370G>T
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NP_001369717.1:p.Glu1124Ter
|
|
NM_001382789.1:c.3361G>T
|
NP_001369718.1:p.Glu1121Ter
|
|
NM_001382790.1:c.3337G>T
|
NP_001369719.1:p.Glu1113Ter
|
|
NM_001382791.1:c.3331G>T
|
NP_001369720.1:p.Glu1111Ter
|
|
NM_001382792.1:c.3304G>T
|
NP_001369721.1:p.Glu1102Ter
|
|
NM_001382793.1:c.3298G>T
|
NP_001369722.1:p.Glu1100Ter
|
|
NM_001382794.1:c.3298G>T
|
NP_001369723.1:p.Glu1100Ter
|
|
NM_001382795.1:c.3292G>T
|
NP_001369724.1:p.Glu1098Ter
|
|
NM_001382796.1:c.3253G>T
|
NP_001369725.1:p.Glu1085Ter
|
|
NM_001382797.1:c.3241G>T
|
NP_001369726.1:p.Glu1081Ter
|
|
NM_001382798.1:c.3184G>T
|
NP_001369727.1:p.Glu1062Ter
|
|
NM_001382799.1:c.3160G>T
|
NP_001369728.1:p.Glu1054Ter
|
|
NM_001382800.1:c.3154G>T
|
NP_001369729.1:p.Glu1052Ter
|
|
NM_001382801.1:c.3136G>T
|
NP_001369730.1:p.Glu1046Ter
|
|
NM_001382802.1:c.3082G>T
|
NP_001369731.1:p.Glu1028Ter
|
|
NM_001382803.1:c.3118-214G>T
|
NP_001369732.1:n.3118-214G>T
|
|
NM_001382804.1:c.2512G>T
|
NP_001369733.1:p.Glu838Ter
|
|
NM_001382805.1:c.2389G>T
|
NP_001369734.1:p.Glu797Ter
|
|
NM_001382806.1:c.2302G>T
|
NP_001369735.1:p.Glu768Ter
|
|
NM_004448.4:c.3340G>T
MANE Select
|
NP_004439.2:p.Glu1114Ter
|
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NR_110535.2:n.3578G>T
|
|
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