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ENST00000265909.9:c.2695A>G
MANE Select
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ENSP00000265909.4:p.Thr899Ala
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ENST00000265909.8:c.2695A>G
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ENSP00000265909.4:p.Thr899Ala
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ENST00000426933.6:c.199A>G
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ENSP00000413345.2:p.Thr67Ala
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ENST00000526579.5:n.178-974A>G
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ENST00000527116.5:n.457A>G
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ENST00000528555.5:c.835A>G
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ENSP00000435122.1:p.Thr279Ala
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ENST00000530330.1:n.431A>G
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ENST00000530356.5:c.835A>G
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ENSP00000432307.1:p.Thr279Ala
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ENST00000533318.5:n.1055A>G
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ENST00000534726.5:c.415A>G
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ENSP00000433699.1:p.Thr139Ala
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NM_001301089.1:c.835A>G
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NP_001288018.1:p.Thr279Ala
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NM_014758.2:c.2695A>G
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NP_055573.2:p.Thr899Ala
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XM_005271546.3:c.2574-974A>G
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XP_005271603.1:n.2574-974A>G
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XM_011542819.1:c.2941A>G
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XP_011541121.1:p.Thr981Ala
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XM_011542820.1:c.2929A>G
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XP_011541122.1:p.Thr977Ala
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XM_011542821.1:c.2821A>G
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XP_011541123.1:p.Thr941Ala
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XM_011542824.1:c.2059A>G
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XP_011541126.1:p.Thr687Ala
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XM_011542825.1:c.1216A>G
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XP_011541127.1:p.Thr406Ala
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XM_011542826.1:c.1081A>G
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XP_011541128.1:p.Thr361Ala
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XM_011542827.1:c.961A>G
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XP_011541129.1:p.Thr321Ala
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NM_001347918.1:c.2575A>G
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NP_001334847.1:p.Thr859Ala
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NM_001347919.1:c.2574-974A>G
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NP_001334848.1:n.2574-974A>G
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NM_001347922.1:c.1024A>G
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NP_001334851.1:p.Thr342Ala
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NM_001347923.1:c.970A>G
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NP_001334852.1:p.Thr324Ala
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NM_001347924.1:c.715A>G
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NP_001334853.1:p.Thr239Ala
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NM_001347925.1:c.661A>G
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NP_001334854.1:p.Thr221Ala
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NM_001347926.1:c.714-974A>G
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NP_001334855.1:n.714-974A>G
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NM_001347927.1:c.415A>G
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NP_001334856.1:p.Thr139Ala
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NR_144939.1:n.3328A>G
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XM_011542820.2:c.2929A>G
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XP_011541122.1:p.Thr977Ala
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XM_011542821.3:c.2821A>G
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XP_011541123.1:p.Thr941Ala
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XM_011542824.2:c.2059A>G
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XP_011541126.1:p.Thr687Ala
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XM_011542825.2:c.1216A>G
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XP_011541127.1:p.Thr406Ala
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XM_011542826.2:c.1081A>G
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XP_011541128.1:p.Thr361Ala
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XM_024448521.1:c.2941A>G
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XP_024304289.1:p.Thr981Ala
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XR_001747870.1:n.3766A>G
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XR_001747872.1:n.3112A>G
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XR_001747873.1:n.3426A>G
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NM_001301089.2:c.835A>G
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NP_001288018.1:p.Thr279Ala
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NM_001347918.2:c.2575A>G
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NP_001334847.2:p.Thr859Ala
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NM_001347919.2:c.2574-974A>G
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NP_001334848.2:n.2574-974A>G
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NM_001347920.2:c.*21091A>G
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NP_001334849.2:n.*21091A>G
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NM_001347922.2:c.1024A>G
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NP_001334851.2:p.Thr342Ala
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NM_001347923.2:c.970A>G
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NP_001334852.2:p.Thr324Ala
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NM_001347924.2:c.715A>G
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NP_001334853.1:p.Thr239Ala
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NM_001347925.2:c.661A>G
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NP_001334854.1:p.Thr221Ala
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NM_001347926.2:c.714-974A>G
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NP_001334855.1:n.714-974A>G
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NM_001347927.2:c.415A>G
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NP_001334856.1:p.Thr139Ala
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NM_014758.3:c.2695A>G
MANE Select
|
NP_055573.3:p.Thr899Ala
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NR_144939.2:n.3320A>G
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