ENST00000278379.9:c.1663G>T
MANE Select
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ENSP00000278379.3:p.Ala555Ser
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ENST00000395750.6:c.1651G>T
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ENSP00000379099.2:p.Ala551Ser
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ENST00000395753.6:c.1636G>T
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ENSP00000379102.1:p.Ala546Ser
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ENST00000479543.2:n.1215G>T
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ENST00000642171.1:c.*45G>T
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ENSP00000495538.1:n.*45G>T
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ENST00000642448.1:n.1755G>T
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ENST00000642769.1:c.929G>T
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ENST00000643000.1:c.1636G>T
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ENSP00000495164.1:p.Ala546Ser
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ENST00000643134.1:c.1654-4G>T
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ENSP00000495188.1:n.1654-4G>T
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ENST00000643522.1:c.1429G>T
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ENSP00000496375.1:p.Ala477Ser
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ENST00000644050.1:c.1636G>T
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ENSP00000496123.1:p.Ala546Ser
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ENST00000644299.1:c.1636G>T
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ENSP00000494669.1:p.Ala546Ser
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ENST00000644459.1:c.*155G>T
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ENSP00000495861.1:n.*155G>T
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ENST00000644779.1:c.1774G>T
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ENSP00000494258.1:p.Ala592Ser
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ENST00000644868.1:c.1725G>T
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ENSP00000496760.1:n.1725G>T
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ENST00000645194.1:c.1636G>T
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ENSP00000496093.1:p.Ala546Ser
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ENST00000645303.1:c.1678G>T
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ENSP00000496667.1:p.Ala560Ser
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ENST00000645542.1:n.369G>T
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ENST00000645634.1:c.1636G>T
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ENSP00000493945.1:p.Ala546Ser
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ENST00000646080.1:c.1654G>T
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ENSP00000494113.1:p.Ala552Ser
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ENST00000647076.1:c.404G>T
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ENST00000647104.1:c.1636G>T
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ENSP00000494025.1:p.Ala546Ser
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ENST00000278379.7:c.1663G>T
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ENSP00000278379.3:p.Ala555Ser
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ENST00000395750.5:c.1636G>T
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ENSP00000379099.1:p.Ala546Ser
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ENST00000395753.5:c.1636G>T
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ENSP00000379102.1:p.Ala546Ser
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ENST00000464522.2:c.219+4571G>T
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ENSP00000435406.1:n.219+4571G>T
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ENST00000479543.1:n.479G>T
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NM_001195728.2:c.1636G>T
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NP_001182657.1:p.Ala546Ser
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NM_001252652.1:c.1636G>T
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NP_001239581.1:p.Ala546Ser
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NM_004171.3:c.1663G>T
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NP_004162.2:p.Ala555Ser
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XM_005253067.1:c.1654G>T
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XP_005253124.1:p.Ala552Ser
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XM_011520284.1:c.1711G>T
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XP_011518586.1:p.Ala571Ser
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XM_011520285.1:c.1651G>T
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XP_011518587.1:p.Ala551Ser
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XM_011520286.1:c.1576G>T
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XP_011518588.1:p.Ala526Ser
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XM_011520287.1:c.1477G>T
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XP_011518589.1:p.Ala493Ser
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XM_011520285.2:c.1651G>T
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XP_011518587.1:p.Ala551Ser
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XM_017018136.1:c.1678G>T
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XP_016873625.1:p.Ala560Ser
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XM_017018137.1:c.1636G>T
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XP_016873626.1:p.Ala546Ser
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XM_017018138.1:c.1636G>T
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XP_016873627.1:p.Ala546Ser
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XM_017018139.1:c.1429G>T
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XP_016873628.1:p.Ala477Ser
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NM_004171.4:c.1663G>T
MANE Select
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NP_004162.2:p.Ala555Ser
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NM_001195728.3:c.1636G>T
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NP_001182657.1:p.Ala546Ser
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NM_001252652.2:c.1636G>T
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NP_001239581.1:p.Ala546Ser
|
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