ENST00000355773.6:c.1285A>G
MANE Select
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ENSP00000348019.5:p.Thr429Ala
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ENST00000355773.5:c.1285A>G
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ENSP00000348019.5:p.Thr429Ala
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NM_012434.4:c.1285A>G
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NP_036566.1:p.Thr429Ala
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XM_005248710.2:c.1234A>G
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XP_005248767.1:p.Thr412Ala
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XM_005248711.1:c.1087A>G
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XP_005248768.1:p.Thr363Ala
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XM_011535750.1:c.1137A>G
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XP_011534052.1:p.Ser379=
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NM_012434.5:c.1285A>G
MANE Select
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NP_036566.1:p.Thr429Ala
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NM_001382629.1:c.1054A>G
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NP_001369558.1:p.Thr352Ala
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NM_001382630.1:c.1260-5202A>G
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NP_001369559.1:n.1260-5202A>G
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NM_001382631.1:c.1306A>G
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NP_001369560.1:p.Thr436Ala
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NM_001382632.1:c.1198A>G
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NP_001369561.1:p.Thr400Ala
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NM_001382633.1:c.1285A>G
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NP_001369562.1:p.Thr429Ala
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NM_001382634.1:c.1126A>G
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NP_001369563.1:p.Thr376Ala
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NM_001382635.1:c.1282A>G
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NP_001369564.1:p.Thr428Ala
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NM_001382636.1:c.967A>G
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NP_001369565.1:p.Thr323Ala
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