ENST00000269571.10:c.3595C>T
MANE Select
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ENSP00000269571.4:p.Pro1199Ser
|
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ENST00000269571.9:c.3595C>T
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ENSP00000269571.4:p.Pro1199Ser
|
|
ENST00000406381.6:c.3505C>T
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ENSP00000385185.2:p.Pro1169Ser
|
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ENST00000445658.6:c.2767C>T
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ENSP00000404047.2:p.Pro923Ser
|
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ENST00000541774.5:c.3550C>T
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ENSP00000446466.1:p.Pro1184Ser
|
|
ENST00000578373.5:c.*3385C>T
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ENSP00000463427.1:n.*3385C>T
|
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ENST00000584450.5:c.*174C>T
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ENSP00000463714.1:n.*174C>T
|
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ENST00000584601.5:c.3505C>T
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ENSP00000462438.1:p.Pro1169Ser
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NM_001005862.2:c.3505C>T , LRG_724t1:c.3505C>T
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NP_001005862.1:p.Pro1169Ser
|
|
NM_001289936.1:c.3550C>T , LRG_724t4:c.3550C>T
|
NP_001276865.1:p.Pro1184Ser
|
|
NM_001289937.1:c.*174C>T
|
NP_001276866.1:n.*174C>T
|
|
NM_004448.3:c.3595C>T , LRG_724t2:c.3595C>T
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NP_004439.2:p.Pro1199Ser
|
|
NR_110535.1:n.3919C>T
|
|
|
XM_024450641.1:c.3733C>T
|
XP_024306409.1:p.Pro1245Ser
|
|
XM_024450642.1:c.3688C>T
|
XP_024306410.1:p.Pro1230Ser
|
|
XM_024450643.1:c.3643C>T
|
XP_024306411.1:p.Pro1215Ser
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|
NM_001005862.3:c.3505C>T
|
NP_001005862.1:p.Pro1169Ser
|
|
NM_001289936.2:c.3550C>T
|
NP_001276865.1:p.Pro1184Ser
|
|
NM_001289937.2:c.*174C>T
|
NP_001276866.1:n.*174C>T
|
|
NM_001382782.1:c.3505C>T
|
NP_001369711.1:p.Pro1169Ser
|
|
NM_001382783.1:c.3505C>T
|
NP_001369712.1:p.Pro1169Ser
|
|
NM_001382784.1:c.3712C>T
|
NP_001369713.1:p.Pro1238Ser
|
|
NM_001382785.1:c.3697C>T
|
NP_001369714.1:p.Pro1233Ser
|
|
NM_001382786.1:c.3676C>T
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NP_001369715.1:p.Pro1226Ser
|
|
NM_001382787.1:c.3670C>T
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NP_001369716.1:p.Pro1224Ser
|
|
NM_001382788.1:c.3625C>T
|
NP_001369717.1:p.Pro1209Ser
|
|
NM_001382789.1:c.3616C>T
|
NP_001369718.1:p.Pro1206Ser
|
|
NM_001382790.1:c.3592C>T
|
NP_001369719.1:p.Pro1198Ser
|
|
NM_001382791.1:c.3586C>T
|
NP_001369720.1:p.Pro1196Ser
|
|
NM_001382792.1:c.3559C>T
|
NP_001369721.1:p.Pro1187Ser
|
|
NM_001382793.1:c.3553C>T
|
NP_001369722.1:p.Pro1185Ser
|
|
NM_001382794.1:c.3553C>T
|
NP_001369723.1:p.Pro1185Ser
|
|
NM_001382795.1:c.3547C>T
|
NP_001369724.1:p.Pro1183Ser
|
|
NM_001382796.1:c.3508C>T
|
NP_001369725.1:p.Pro1170Ser
|
|
NM_001382797.1:c.3496C>T
|
NP_001369726.1:p.Pro1166Ser
|
|
NM_001382798.1:c.3439C>T
|
NP_001369727.1:p.Pro1147Ser
|
|
NM_001382799.1:c.3415C>T
|
NP_001369728.1:p.Pro1139Ser
|
|
NM_001382800.1:c.3409C>T
|
NP_001369729.1:p.Pro1137Ser
|
|
NM_001382801.1:c.3391C>T
|
NP_001369730.1:p.Pro1131Ser
|
|
NM_001382802.1:c.3337C>T
|
NP_001369731.1:p.Pro1113Ser
|
|
NM_001382803.1:c.*174C>T
|
NP_001369732.1:n.*174C>T
|
|
NM_001382804.1:c.2767C>T
|
NP_001369733.1:p.Pro923Ser
|
|
NM_001382805.1:c.2644C>T
|
NP_001369734.1:p.Pro882Ser
|
|
NM_001382806.1:c.2557C>T
|
NP_001369735.1:p.Pro853Ser
|
|
NM_004448.4:c.3595C>T
MANE Select
|
NP_004439.2:p.Pro1199Ser
|
|
NR_110535.2:n.3833C>T
|
|
|