ENST00000261884.8:c.1194C>T
MANE Select
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ENSP00000261884.3:p.Ala398=
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ENST00000261884.7:c.1194C>T
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ENSP00000261884.3:p.Ala398=
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ENST00000560475.1:c.111+8736C>T
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ENST00000560567.5:c.1067C>T
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ENSP00000453106.1:p.Pro356Leu
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NM_016213.4:c.1194C>T
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NP_057297.2:p.Ala398=
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XM_005254789.1:c.504C>T
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XP_005254846.1:p.Ala168=
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XR_243130.1:n.1125C>T
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NM_001321924.1:c.504C>T
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NP_001308853.1:p.Ala168=
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NR_135855.1:n.1127C>T
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NM_001321924.2:c.504C>T
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NP_001308853.1:p.Ala168=
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NM_016213.5:c.1194C>T
MANE Select
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NP_057297.2:p.Ala398=
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NR_135855.2:n.1095C>T
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