ENST00000269571.10:c.3590T>G
MANE Select
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ENSP00000269571.4:p.Leu1197Trp
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ENST00000269571.9:c.3590T>G
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ENSP00000269571.4:p.Leu1197Trp
|
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ENST00000406381.6:c.3500T>G
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ENSP00000385185.2:p.Leu1167Trp
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ENST00000445658.6:c.2762T>G
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ENSP00000404047.2:p.Leu921Trp
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ENST00000541774.5:c.3545T>G
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ENSP00000446466.1:p.Leu1182Trp
|
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ENST00000578373.5:c.*3380T>G
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ENSP00000463427.1:n.*3380T>G
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ENST00000584450.5:c.*169T>G
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ENSP00000463714.1:n.*169T>G
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|
ENST00000584601.5:c.3500T>G
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ENSP00000462438.1:p.Leu1167Trp
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NM_001005862.2:c.3500T>G , LRG_724t1:c.3500T>G
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NP_001005862.1:p.Leu1167Trp
|
|
NM_001289936.1:c.3545T>G , LRG_724t4:c.3545T>G
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NP_001276865.1:p.Leu1182Trp
|
|
NM_001289937.1:c.*169T>G
|
NP_001276866.1:n.*169T>G
|
|
NM_004448.3:c.3590T>G , LRG_724t2:c.3590T>G
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NP_004439.2:p.Leu1197Trp
|
|
NR_110535.1:n.3914T>G
|
|
|
XM_024450641.1:c.3728T>G
|
XP_024306409.1:p.Leu1243Trp
|
|
XM_024450642.1:c.3683T>G
|
XP_024306410.1:p.Leu1228Trp
|
|
XM_024450643.1:c.3638T>G
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XP_024306411.1:p.Leu1213Trp
|
|
NM_001005862.3:c.3500T>G
|
NP_001005862.1:p.Leu1167Trp
|
|
NM_001289936.2:c.3545T>G
|
NP_001276865.1:p.Leu1182Trp
|
|
NM_001289937.2:c.*169T>G
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NP_001276866.1:n.*169T>G
|
|
NM_001382782.1:c.3500T>G
|
NP_001369711.1:p.Leu1167Trp
|
|
NM_001382783.1:c.3500T>G
|
NP_001369712.1:p.Leu1167Trp
|
|
NM_001382784.1:c.3707T>G
|
NP_001369713.1:p.Leu1236Trp
|
|
NM_001382785.1:c.3692T>G
|
NP_001369714.1:p.Leu1231Trp
|
|
NM_001382786.1:c.3671T>G
|
NP_001369715.1:p.Leu1224Trp
|
|
NM_001382787.1:c.3665T>G
|
NP_001369716.1:p.Leu1222Trp
|
|
NM_001382788.1:c.3620T>G
|
NP_001369717.1:p.Leu1207Trp
|
|
NM_001382789.1:c.3611T>G
|
NP_001369718.1:p.Leu1204Trp
|
|
NM_001382790.1:c.3587T>G
|
NP_001369719.1:p.Leu1196Trp
|
|
NM_001382791.1:c.3581T>G
|
NP_001369720.1:p.Leu1194Trp
|
|
NM_001382792.1:c.3554T>G
|
NP_001369721.1:p.Leu1185Trp
|
|
NM_001382793.1:c.3548T>G
|
NP_001369722.1:p.Leu1183Trp
|
|
NM_001382794.1:c.3548T>G
|
NP_001369723.1:p.Leu1183Trp
|
|
NM_001382795.1:c.3542T>G
|
NP_001369724.1:p.Leu1181Trp
|
|
NM_001382796.1:c.3503T>G
|
NP_001369725.1:p.Leu1168Trp
|
|
NM_001382797.1:c.3491T>G
|
NP_001369726.1:p.Leu1164Trp
|
|
NM_001382798.1:c.3434T>G
|
NP_001369727.1:p.Leu1145Trp
|
|
NM_001382799.1:c.3410T>G
|
NP_001369728.1:p.Leu1137Trp
|
|
NM_001382800.1:c.3404T>G
|
NP_001369729.1:p.Leu1135Trp
|
|
NM_001382801.1:c.3386T>G
|
NP_001369730.1:p.Leu1129Trp
|
|
NM_001382802.1:c.3332T>G
|
NP_001369731.1:p.Leu1111Trp
|
|
NM_001382803.1:c.*169T>G
|
NP_001369732.1:n.*169T>G
|
|
NM_001382804.1:c.2762T>G
|
NP_001369733.1:p.Leu921Trp
|
|
NM_001382805.1:c.2639T>G
|
NP_001369734.1:p.Leu880Trp
|
|
NM_001382806.1:c.2552T>G
|
NP_001369735.1:p.Leu851Trp
|
|
NM_004448.4:c.3590T>G
MANE Select
|
NP_004439.2:p.Leu1197Trp
|
|
NR_110535.2:n.3828T>G
|
|
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