ENST00000340855.11:c.894G>C
MANE Select
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ENSP00000339801.6:p.Gln298His
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ENST00000651111.1:c.261G>C
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ENSP00000498395.1:p.Gln87His
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ENST00000340855.10:c.894G>C
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ENSP00000339801.6:p.Gln298His
|
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ENST00000370441.8:c.894G>C
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ENSP00000359470.4:p.Gln298His
|
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ENST00000422081.6:c.261G>C
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ENSP00000477056.1:p.Gln87His
|
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ENST00000441880.1:n.114-3328G>C
|
|
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ENST00000464251.5:c.820G>C
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ENSP00000428980.1:n.820G>C
|
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ENST00000466323.5:c.*85G>C
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ENSP00000418264.1:n.*85G>C
|
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ENST00000490775.5:n.679G>C
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|
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NM_000202.6:c.894G>C
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NP_000193.1:p.Gln298His
|
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NM_001166550.2:c.624G>C
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NP_001160022.1:p.Gln208His
|
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NM_006123.4:c.894G>C
|
NP_006114.1:p.Gln298His
|
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NR_104128.1:n.1241G>C
|
|
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NM_000202.7:c.894G>C
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NP_000193.1:p.Gln298His
|
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NM_001166550.3:c.624G>C
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NP_001160022.1:p.Gln208His
|
|
NM_000202.8:c.894G>C
MANE Select
|
NP_000193.1:p.Gln298His
|
|
NM_001166550.4:c.624G>C
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NP_001160022.1:p.Gln208His
|
|
NM_006123.5:c.894G>C
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NP_006114.1:p.Gln298His
|
|
NR_104128.2:n.1193G>C
|
|
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