ENST00000324001.8:c.2358C>T
MANE Select
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ENSP00000326018.6:p.Ala786=
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ENST00000673881.1:c.1941C>T
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ENSP00000501070.1:p.Ala647=
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ENST00000674005.2:c.2643C>T
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ENSP00000501261.1:p.Ala881=
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ENST00000674773.1:c.1941C>T
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ENSP00000502579.1:p.Ala647=
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ENST00000675517.1:c.2233C>T
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ENST00000676076.1:c.2219C>T
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|
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ENST00000676260.1:c.2320C>T
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ENST00000676316.1:c.2245C>T
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|
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ENST00000291825.11:c.*2563C>T
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ENSP00000291825.6:n.*2563C>T
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ENST00000324001.7:c.2358C>T
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ENSP00000326018.6:p.Ala786=
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NM_020956.2:c.*2563C>T , LRG_265t1:c.*2563C>T
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NP_066007.1:n.*2563C>T
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NM_181882.2:c.2358C>T , LRG_265t2:c.2358C>T
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NP_870998.2:p.Ala786=
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XM_011527171.1:c.2358C>T
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XP_011525473.1:p.Ala786=
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XM_011527171.2:c.2358C>T
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XP_011525473.1:p.Ala786=
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XM_017027046.1:c.2256C>T
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XP_016882535.1:p.Ala752=
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XM_017027047.1:c.2256C>T
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XP_016882536.1:p.Ala752=
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NM_181882.3:c.2358C>T
MANE Select
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NP_870998.2:p.Ala786=
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