ENST00000291281.9:c.513C>T
MANE Select
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ENSP00000291281.3:p.Gly171=
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ENST00000291281.8:c.513C>T
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ENSP00000291281.3:p.Gly171=
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ENST00000433867.5:c.513C>T
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ENSP00000393978.1:p.Gly171=
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ENST00000595132.5:c.42C>T
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ENSP00000470363.1:p.Gly14=
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ENST00000595515.5:c.513C>T
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ENSP00000470804.1:p.Gly171=
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ENST00000597641.1:c.248C>T
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ENSP00000469064.1:n.248C>T
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ENST00000598633.1:c.42C>T
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ENSP00000470919.1:p.Gly14=
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ENST00000600194.5:c.42C>T
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ENSP00000472744.1:p.Gly14=
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ENST00000601605.5:c.41-3536C>T
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ENSP00000470442.1:n.41-3536C>T
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ENST00000601806.5:c.42C>T
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ENSP00000469106.1:p.Gly14=
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NM_001079880.1:c.513C>T
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NP_001073349.1:p.Gly171=
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NM_001079881.1:c.513C>T
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NP_001073350.1:p.Gly171=
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NM_001079882.1:c.42C>T
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NP_001073351.1:p.Gly14=
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NM_016457.4:c.513C>T
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NP_057541.2:p.Gly171=
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XM_005258716.2:c.42C>T
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XP_005258773.2:p.Gly14=
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NM_001079880.2:c.513C>T
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NP_001073349.1:p.Gly171=
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NM_001079881.2:c.513C>T
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NP_001073350.1:p.Gly171=
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NM_001079882.2:c.42C>T
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NP_001073351.1:p.Gly14=
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NM_016457.5:c.513C>T
MANE Select
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NP_057541.2:p.Gly171=
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