ENST00000326828.6:c.416C>T
MANE Select
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ENSP00000315602.5:p.Ala139Val
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ENST00000326828.5:c.416C>T
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ENSP00000315602.5:p.Ala139Val
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|
ENST00000348639.7:c.416C>T
|
ENSP00000267951.4:p.Ala139Val
|
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ENST00000558903.1:n.123C>T
|
|
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ENST00000559658.5:c.416C>T
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ENSP00000452896.1:p.Ala139Val
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NM_000743.4:c.416C>T
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NP_000734.2:p.Ala139Val
|
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NM_001166694.1:c.416C>T
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NP_001160166.1:p.Ala139Val
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NR_046313.1:n.917C>T
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|
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XM_006720382.1:c.215C>T
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XP_006720445.1:p.Ala72Val
|
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XM_011521173.1:c.335C>T
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XP_011519475.1:p.Ala112Val
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XM_006720382.3:c.215C>T
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XP_006720445.1:p.Ala72Val
|
|
NM_000743.5:c.416C>T
MANE Select
|
NP_000734.2:p.Ala139Val
|
|
NM_001166694.2:c.416C>T
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NP_001160166.1:p.Ala139Val
|
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NR_046313.2:n.618C>T
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