ENST00000644719.2:c.675G>A
MANE Select
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ENSP00000496625.1:p.Arg225=
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ENST00000418967.6:c.675G>A
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ENSP00000408860.2:p.Arg225=
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|
ENST00000435122.3:c.585G>A
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ENSP00000415043.2:p.Arg195=
|
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ENST00000462278.1:n.364G>A
|
|
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ENST00000466779.5:c.*367G>A
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ENSP00000417321.1:n.*367G>A
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ENST00000466879.5:n.726G>A
|
|
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ENST00000479074.5:n.733G>A
|
|
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ENST00000479730.5:n.791G>A
|
|
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ENST00000483041.5:n.844G>A
|
|
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ENST00000486063.5:n.855G>A
|
|
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NM_000500.7:c.675G>A
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NP_000491.4:p.Arg225=
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|
NM_001128590.3:c.585G>A
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NP_001122062.3:p.Arg195=
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XM_011514314.1:c.270G>A
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XP_011512616.1:p.Arg90=
|
|
NM_000500.9:c.675G>A
MANE Select
|
NP_000491.4:p.Arg225=
|
|
NM_001368143.1:c.270G>A
|
NP_001355072.1:p.Arg90=
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|
NM_001368144.1:c.270G>A
|
NP_001355073.1:p.Arg90=
|
|
NM_001128590.4:c.585G>A
|
NP_001122062.3:p.Arg195=
|
|
NM_001368143.2:c.270G>A
|
NP_001355072.1:p.Arg90=
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NM_001368144.2:c.270G>A
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NP_001355073.1:p.Arg90=
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