ENST00000301761.7:c.430G>T
MANE Select
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ENSP00000301761.3:p.Ala144Ser
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ENST00000301761.6:c.430G>T
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ENSP00000301761.2:p.Ala144Ser
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ENST00000359614.9:c.*138G>T
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ENSP00000352630.5:n.*138G>T
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ENST00000536670.5:n.396+7887G>T
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|
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ENST00000537782.5:c.*76G>T
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ENSP00000469951.1:n.*76G>T
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ENST00000538594.5:c.370+7887G>T
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ENSP00000440939.1:n.370+7887G>T
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ENST00000541135.5:c.377+7880G>T
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ENSP00000443130.1:n.377+7880G>T
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ENST00000542074.1:c.*9G>T
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ENSP00000469670.1:n.*9G>T
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ENST00000542794.5:c.*432G>T
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ENSP00000439983.1:n.*432G>T
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ENST00000543044.2:c.394G>T
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ENSP00000440219.1:p.Ala132Ser
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|
ENST00000543265.1:c.*53G>T
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ENSP00000443660.1:n.*53G>T
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ENST00000544025.5:n.465+7887G>T
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|
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ENST00000544801.5:c.370+7887G>T
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ENSP00000442581.1:n.370+7887G>T
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ENST00000544880.1:n.374+7887G>T
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|
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NM_017841.2:c.430G>T , LRG_519t1:c.430G>T
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NP_060311.1:p.Ala144Ser
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NM_017841.4:c.430G>T
MANE Select
|
NP_060311.1:p.Ala144Ser
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