ENST00000309755.9:c.1020A>T
MANE Select
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ENSP00000312397.4:p.Ala340=
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ENST00000309755.8:c.1020A>T
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ENSP00000312397.4:p.Ala340=
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ENST00000502381.1:n.607A>T
|
|
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ENST00000504208.5:c.*335-11424A>T
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ENSP00000423585.1:n.*335-11424A>T
|
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ENST00000505853.1:c.900A>T
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ENSP00000426173.1:p.Ala300=
|
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ENST00000506491.5:c.774A>T
|
ENSP00000424828.1:p.Ala258=
|
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ENST00000506873.5:n.645A>T
|
|
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ENST00000508657.5:c.924A>T
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ENSP00000422099.1:p.Ala308=
|
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NM_001257194.1:c.924A>T
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NP_001244123.1:p.Ala308=
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NM_001257195.1:c.774A>T
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NP_001244124.1:p.Ala258=
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NM_017415.2:c.1020A>T
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NP_059111.2:p.Ala340=
|
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NM_017415.3:c.1020A>T
MANE Select
|
NP_059111.2:p.Ala340=
|
|
NM_001257195.2:c.774A>T
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NP_001244124.1:p.Ala258=
|
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