ENST00000340855.11:c.893A>G
MANE Select
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ENSP00000339801.6:p.Gln298Arg
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ENST00000651111.1:c.260A>G
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ENSP00000498395.1:p.Gln87Arg
|
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ENST00000340855.10:c.893A>G
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ENSP00000339801.6:p.Gln298Arg
|
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ENST00000370441.8:c.893A>G
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ENSP00000359470.4:p.Gln298Arg
|
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ENST00000422081.6:c.260A>G
|
ENSP00000477056.1:p.Gln87Arg
|
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ENST00000441880.1:n.114-3329A>G
|
|
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ENST00000464251.5:c.819A>G
|
ENSP00000428980.1:n.819A>G
|
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ENST00000466323.5:c.*84A>G
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ENSP00000418264.1:n.*84A>G
|
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ENST00000490775.5:n.678A>G
|
|
|
NM_000202.6:c.893A>G
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NP_000193.1:p.Gln298Arg
|
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NM_001166550.2:c.623A>G
|
NP_001160022.1:p.Gln208Arg
|
|
NM_006123.4:c.893A>G
|
NP_006114.1:p.Gln298Arg
|
|
NR_104128.1:n.1240A>G
|
|
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NM_000202.7:c.893A>G
|
NP_000193.1:p.Gln298Arg
|
|
NM_001166550.3:c.623A>G
|
NP_001160022.1:p.Gln208Arg
|
|
NM_000202.8:c.893A>G
MANE Select
|
NP_000193.1:p.Gln298Arg
|
|
NM_001166550.4:c.623A>G
|
NP_001160022.1:p.Gln208Arg
|
|
NM_006123.5:c.893A>G
|
NP_006114.1:p.Gln298Arg
|
|
NR_104128.2:n.1192A>G
|
|
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