ENST00000295897.9:c.1768A>G
MANE Select
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ENSP00000295897.4:p.Thr590Ala
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ENST00000295897.8:c.1768A>G
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ENSP00000295897.4:p.Thr590Ala
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ENST00000401494.7:c.1423A>G
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ENSP00000384695.3:p.Thr475Ala
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ENST00000415165.6:c.1192A>G
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ENSP00000401820.2:p.Thr398Ala
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ENST00000476441.6:c.*1047A>G
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ENSP00000423727.1:n.*1047A>G
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ENST00000495173.1:n.76A>G
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ENST00000503124.5:c.1318A>G
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ENSP00000421027.1:p.Thr440Ala
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ENST00000505649.5:n.1315A>G
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ENST00000508932.5:n.175+167A>G
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ENST00000509063.5:c.1768A>G
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ENSP00000422784.1:p.Thr590Ala
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ENST00000511370.1:c.1301A>G
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ENST00000621085.4:c.1129A>G
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ENSP00000483421.1:p.Thr377Ala
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ENST00000621628.4:c.1129A>G
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ENSP00000480485.1:p.Thr377Ala
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NM_000477.5:c.1768A>G
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NP_000468.1:p.Thr590Ala
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NM_000477.6:c.1768A>G
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NP_000468.1:p.Thr590Ala
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NM_000477.7:c.1768A>G
MANE Select
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NP_000468.1:p.Thr590Ala
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