ENST00000296589.9:c.797A>G
MANE Select
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ENSP00000296589.4:p.Tyr266Cys
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ENST00000296589.8:c.797A>G
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ENSP00000296589.4:p.Tyr266Cys
|
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ENST00000382102.7:c.797A>G
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ENSP00000371534.3:p.Tyr266Cys
|
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ENST00000505056.1:n.599A>G
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|
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ENST00000509381.1:c.563-9278A>G
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ENSP00000421100.1:n.563-9278A>G
|
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ENST00000510600.1:c.272A>G
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ENSP00000424010.1:p.Tyr91Cys
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NM_001012509.3:c.797A>G
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NP_001012527.1:p.Tyr266Cys
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NM_001297417.2:c.563-9278A>G
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NP_001284346.2:n.563-9278A>G
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NM_016180.4:c.797A>G
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NP_057264.3:p.Tyr266Cys
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XM_011514051.1:c.395A>G
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XP_011512353.1:p.Tyr132Cys
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XM_011514052.1:c.797A>G
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XP_011512354.1:p.Tyr266Cys
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XR_925620.1:n.1614A>G
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|
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NM_016180.5:c.797A>G
MANE Select
|
NP_057264.4:p.Tyr266Cys
|
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NM_001012509.4:c.797A>G
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NP_001012527.2:p.Tyr266Cys
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NM_001297417.3:c.563-9278A>G
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NP_001284346.2:n.563-9278A>G
|
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NM_001297417.4:c.563-9278A>G
|
NP_001284346.2:n.563-9278A>G
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