ENST00000307363.10:c.382G>T
MANE Select
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ENSP00000306920.4:p.Ala128Ser
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ENST00000307363.9:c.382G>T
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ENSP00000306920.4:p.Ala128Ser
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ENST00000307377.12:c.246-3277G>T
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ENSP00000305920.8:n.246-3277G>T
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ENST00000399402.7:c.292G>T
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ENSP00000382333.2:p.Ala98Ser
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ENST00000415454.1:c.76-10565G>T
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ENSP00000411813.1:n.76-10565G>T
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ENST00000438227.1:c.76-3277G>T
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ENSP00000401250.1:n.76-3277G>T
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ENST00000440656.1:c.-12G>T
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ENSP00000411769.1:n.-12G>T
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ENST00000446732.5:c.156-3277G>T
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ENSP00000407365.1:n.156-3277G>T
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ENST00000450835.1:c.292G>T
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ENSP00000403264.1:p.Ala98Ser
|
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ENST00000464355.1:n.340G>T
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|
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ENST00000482097.5:n.109-15285G>T
|
|
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ENST00000485698.5:n.137-15285G>T
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|
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ENST00000498537.5:n.133-15285G>T
|
|
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NM_000404.2:c.382G>T
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NP_000395.2:p.Ala128Ser
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NM_000404.3:c.382G>T
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NP_000395.2:p.Ala128Ser
|
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NM_001079811.1:c.292G>T
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NP_001073279.1:p.Ala98Ser
|
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NM_001079811.2:c.292G>T
|
NP_001073279.1:p.Ala98Ser
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NM_001135602.1:c.246-3277G>T
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NP_001129074.1:n.246-3277G>T
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NM_001135602.2:c.246-3277G>T
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NP_001129074.1:n.246-3277G>T
|
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NM_001317040.1:c.526G>T
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NP_001303969.1:p.Ala176Ser
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NM_000404.4:c.382G>T
MANE Select
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NP_000395.3:p.Ala128Ser
|
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NM_001079811.3:c.292G>T
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NP_001073279.2:p.Ala98Ser
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NM_001135602.3:c.246-3277G>T
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NP_001129074.2:n.246-3277G>T
|
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NM_001317040.2:c.526G>T
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NP_001303969.2:p.Ala176Ser
|
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NM_001393580.1:c.382G>T
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NP_001380509.1:p.Ala128Ser
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