ENST00000296589.9:c.887A>G
MANE Select
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ENSP00000296589.4:p.Gln296Arg
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ENST00000296589.8:c.887A>G
|
ENSP00000296589.4:p.Gln296Arg
|
|
ENST00000382102.7:c.887A>G
|
ENSP00000371534.3:p.Gln296Arg
|
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ENST00000505056.1:n.689A>G
|
|
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ENST00000509381.1:c.563-9188A>G
|
ENSP00000421100.1:n.563-9188A>G
|
|
ENST00000510600.1:c.362A>G
|
ENSP00000424010.1:p.Gln121Arg
|
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NM_001012509.3:c.887A>G
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NP_001012527.1:p.Gln296Arg
|
|
NM_001297417.2:c.563-9188A>G
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NP_001284346.2:n.563-9188A>G
|
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NM_016180.4:c.887A>G
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NP_057264.3:p.Gln296Arg
|
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XM_011514051.1:c.485A>G
|
XP_011512353.1:p.Gln162Arg
|
|
XM_011514052.1:c.887A>G
|
XP_011512354.1:p.Gln296Arg
|
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XR_925620.1:n.1704A>G
|
|
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NM_016180.5:c.887A>G
MANE Select
|
NP_057264.4:p.Gln296Arg
|
|
NM_001012509.4:c.887A>G
|
NP_001012527.2:p.Gln296Arg
|
|
NM_001297417.3:c.563-9188A>G
|
NP_001284346.2:n.563-9188A>G
|
|
NM_001297417.4:c.563-9188A>G
|
NP_001284346.2:n.563-9188A>G
|
|