ENST00000340855.11:c.586T>G
MANE Select
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ENSP00000339801.6:p.Leu196Val
|
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ENST00000651111.1:c.-48T>G
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ENSP00000498395.1:n.-48T>G
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ENST00000340855.10:c.586T>G
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ENSP00000339801.6:p.Leu196Val
|
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ENST00000370441.8:c.586T>G
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ENSP00000359470.4:p.Leu196Val
|
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ENST00000422081.6:c.-48T>G
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ENSP00000477056.1:n.-48T>G
|
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ENST00000441880.1:n.114-11131T>G
|
|
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ENST00000464251.5:c.512T>G
|
ENSP00000428980.1:n.512T>G
|
|
ENST00000466019.1:n.38T>G
|
|
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ENST00000466323.5:c.586T>G
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ENSP00000418264.1:p.Leu196Val
|
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ENST00000490775.5:n.371T>G
|
|
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ENST00000523759.5:n.700T>G
|
|
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NM_000202.6:c.586T>G
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NP_000193.1:p.Leu196Val
|
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NM_001166550.2:c.316T>G
|
NP_001160022.1:p.Leu106Val
|
|
NM_006123.4:c.586T>G
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NP_006114.1:p.Leu196Val
|
|
NR_104128.1:n.803T>G
|
|
|
NM_000202.7:c.586T>G
|
NP_000193.1:p.Leu196Val
|
|
NM_001166550.3:c.316T>G
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NP_001160022.1:p.Leu106Val
|
|
NM_000202.8:c.586T>G
MANE Select
|
NP_000193.1:p.Leu196Val
|
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NM_001166550.4:c.316T>G
|
NP_001160022.1:p.Leu106Val
|
|
NM_006123.5:c.586T>G
|
NP_006114.1:p.Leu196Val
|
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NR_104128.2:n.755T>G
|
|
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