ENST00000355773.6:c.1298C>T
MANE Select
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ENSP00000348019.5:p.Ala433Val
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ENST00000355773.5:c.1298C>T
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ENSP00000348019.5:p.Ala433Val
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NM_012434.4:c.1298C>T
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NP_036566.1:p.Ala433Val
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XM_005248710.2:c.1247C>T
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XP_005248767.1:p.Ala416Val
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XM_005248711.1:c.1100C>T
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XP_005248768.1:p.Ala367Val
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XM_011535750.1:c.1150C>T
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XP_011534052.1:p.Pro384Ser
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NM_012434.5:c.1298C>T
MANE Select
|
NP_036566.1:p.Ala433Val
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NM_001382629.1:c.1067C>T
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NP_001369558.1:p.Ala356Val
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NM_001382630.1:c.1260-5189C>T
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NP_001369559.1:n.1260-5189C>T
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NM_001382631.1:c.1319C>T
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NP_001369560.1:p.Ala440Val
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NM_001382632.1:c.1211C>T
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NP_001369561.1:p.Ala404Val
|
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NM_001382633.1:c.1298C>T
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NP_001369562.1:p.Ala433Val
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NM_001382634.1:c.1139C>T
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NP_001369563.1:p.Ala380Val
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NM_001382635.1:c.1295C>T
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NP_001369564.1:p.Ala432Val
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NM_001382636.1:c.980C>T
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NP_001369565.1:p.Ala327Val
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