ENST00000340855.11:c.287G>A
MANE Select
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ENSP00000339801.6:p.Arg96Lys
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ENST00000651111.1:c.-215-2406G>A
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ENSP00000498395.1:n.-215-2406G>A
|
|
ENST00000340855.10:c.287G>A
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ENSP00000339801.6:p.Arg96Lys
|
|
ENST00000370441.8:c.287G>A
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ENSP00000359470.4:p.Arg96Lys
|
|
ENST00000422081.6:c.-215-2406G>A
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ENSP00000477056.1:n.-215-2406G>A
|
|
ENST00000427113.2:n.770-1220G>A
|
|
|
ENST00000428056.6:c.287G>A
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ENSP00000390241.2:p.Arg96Lys
|
|
ENST00000441880.1:n.114-16345G>A
|
|
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ENST00000464251.5:c.110G>A
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ENSP00000428980.1:p.Arg37Lys
|
|
ENST00000466323.5:c.287G>A
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ENSP00000418264.1:p.Arg96Lys
|
|
ENST00000523759.5:n.533-2406G>A
|
|
|
NM_000202.6:c.287G>A
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NP_000193.1:p.Arg96Lys
|
|
NM_001166550.2:c.17G>A
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NP_001160022.1:p.Arg6Lys
|
|
NM_006123.4:c.287G>A
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NP_006114.1:p.Arg96Lys
|
|
NR_104128.1:n.504G>A
|
|
|
NM_000202.7:c.287G>A
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NP_000193.1:p.Arg96Lys
|
|
NM_001166550.3:c.17G>A
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NP_001160022.1:p.Arg6Lys
|
|
NM_000202.8:c.287G>A
MANE Select
|
NP_000193.1:p.Arg96Lys
|
|
NM_001166550.4:c.17G>A
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NP_001160022.1:p.Arg6Lys
|
|
NM_006123.5:c.287G>A
|
NP_006114.1:p.Arg96Lys
|
|
NR_104128.2:n.456G>A
|
|
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