ENST00000426151.7:c.1287A>T
MANE Select
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ENSP00000389295.1:p.Ala429=
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ENST00000649521.1:c.1335A>T
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ENSP00000497687.1:p.Ala445=
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ENST00000359558.6:c.1389A>T
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ENSP00000352561.2:p.Ala463=
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ENST00000360249.8:c.*797A>T
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ENSP00000353385.5:n.*797A>T
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ENST00000394441.5:c.1287A>T
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ENSP00000377959.1:p.Ala429=
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ENST00000415529.2:c.1337A>T
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ENSP00000413179.1:n.1337A>T
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ENST00000421592.5:c.1335A>T
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ENSP00000399552.1:p.Ala445=
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ENST00000423724.5:c.1385A>T
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ENSP00000391369.1:n.1385A>T
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ENST00000426151.5:c.1287A>T
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ENSP00000389295.1:p.Ala429=
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NM_001164737.1:c.1389A>T
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NP_001158209.1:p.Ala463=
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NM_001164738.1:c.1287A>T
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NP_001158210.1:p.Ala429=
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NM_001742.3:c.1287A>T
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NP_001733.1:p.Ala429=
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NM_001164737.2:c.1335A>T
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NP_001158209.2:p.Ala445=
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NM_001742.4:c.1287A>T
MANE Select
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NP_001733.1:p.Ala429=
|
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NM_001164737.3:c.1335A>T
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NP_001158209.2:p.Ala445=
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NM_001164738.2:c.1287A>T
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NP_001158210.1:p.Ala429=
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