ENST00000256906.5:c.831_834delinsTTCC
MANE Select
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ENSP00000256906.4:p.Gly277=
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ENST00000256906.4:c.831_834delinsTTCC
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ENSP00000256906.4:p.Gly277=
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ENST00000426880.2:c.567_570delinsTTCC
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ENSP00000402526.2:p.Gly189=
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NM_001143828.1:c.567_570delinsTTCC
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NP_001137300.1:p.Gly189=
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NM_001160166.1:c.*463_*466delinsTTCC
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NP_001153638.1:n.*463_*466delinsTTCC
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NM_021624.3:c.831_834delinsTTCC
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NP_067637.2:p.Gly277=
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XM_011526133.1:c.357+8269_357+8272delinsTTCC
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XP_011524435.1:n.357+8269_357+8272delinsTTCC
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NM_021624.4:c.831_834delinsTTCC
MANE Select
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NP_067637.2:p.Gly277=
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NM_001143828.2:c.567_570delinsTTCC
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NP_001137300.1:p.Gly189=
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NM_001160166.2:c.*463_*466delinsTTCC
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NP_001153638.1:n.*463_*466delinsTTCC
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