ENST00000368666.7:c.955T>G
MANE Select
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ENSP00000357655.4:p.Cys319Gly
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ENST00000639360.1:c.856T>G
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ENSP00000491774.1:p.Cys286Gly
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ENST00000230529.9:c.955T>G
|
ENSP00000230529.5:p.Cys319Gly
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ENST00000361714.5:c.955T>G
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ENSP00000354734.2:p.Cys319Gly
|
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ENST00000368663.4:c.*261T>G
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ENSP00000357652.4:n.*261T>G
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ENST00000368664.7:c.*359T>G
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ENSP00000357653.3:n.*359T>G
|
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ENST00000368666.6:c.1009T>G
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ENSP00000357655.3:p.Cys337Gly
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ENST00000409166.5:c.283T>G
|
ENSP00000386467.1:p.Cys95Gly
|
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ENST00000454589.5:c.*359T>G
|
ENSP00000395928.1:n.*359T>G
|
|
ENST00000604763.5:c.955T>G
|
ENSP00000473777.1:p.Cys319Gly
|
|
ENST00000613648.1:n.790T>G
|
|
|
ENST00000620524.3:n.886T>G
|
|
|
NM_003880.3:c.955T>G
|
NP_003871.1:p.Cys319Gly
|
|
NM_198239.1:c.1009T>G
|
NP_937882.1:p.Cys337Gly
|
|
NR_125353.1:n.1209T>G
|
|
|
NR_125354.1:n.1129T>G
|
|
|
XM_011536220.1:c.955T>G
|
XP_011534522.1:p.Cys319Gly
|
|
XM_011536221.1:c.*359T>G
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XP_011534523.1:n.*359T>G
|
|
XM_011536223.1:c.373T>G
|
XP_011534525.1:p.Cys125Gly
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XM_011536223.3:c.373T>G
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XP_011534525.1:p.Cys125Gly
|
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XR_001743705.1:n.1557T>G
|
|
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NM_003880.4:c.955T>G
|
NP_003871.1:p.Cys319Gly
|
|
NM_198239.2:c.955T>G
MANE Select
|
NP_937882.2:p.Cys319Gly
|
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NR_125353.2:n.1273T>G
|
|
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NR_125354.3:n.1100T>G
|
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