ENST00000356141.9:c.1882G>T
MANE Select
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ENSP00000348460.4:p.Ala628Ser
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ENST00000551634.6:c.1891G>T
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ENSP00000448373.2:p.Ala631Ser
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ENST00000680362.1:c.1782G>T
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ENST00000681323.1:c.793+2608G>T
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ENST00000346562.6:c.1786G>T
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ENSP00000319610.5:p.Ala596Ser
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ENST00000356141.8:c.1882G>T
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ENSP00000348460.4:p.Ala628Ser
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ENST00000357798.9:c.1843G>T
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ENSP00000350446.5:p.Ala615Ser
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ENST00000548645.5:c.1792G>T
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ENSP00000448916.1:p.Ala598Ser
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ENST00000551492.5:c.1897G>T
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ENSP00000450392.1:p.Ala633Ser
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ENST00000551634.5:c.1804G>T
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ENSP00000448373.1:p.Ala602Ser
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NM_001164749.1:c.1882G>T
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NP_001158221.1:p.Ala628Ser
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NM_001165893.1:c.1792G>T
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NP_001159365.1:p.Ala598Ser
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NM_022123.2:c.1786G>T
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NP_071406.1:p.Ala596Ser
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NM_173159.2:c.1843G>T
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NP_775182.1:p.Ala615Ser
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XM_005267991.2:c.1903G>T
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XP_005268048.1:p.Ala635Ser
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XM_005267992.2:c.1897G>T
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XP_005268049.1:p.Ala633Ser
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XM_005267993.2:c.1843G>T
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XP_005268050.1:p.Ala615Ser
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XM_011537067.1:c.1933G>T
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XP_011535369.1:p.Ala645Ser
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XM_011537068.1:c.1924G>T
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XP_011535370.1:p.Ala642Ser
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XM_011537069.1:c.1894G>T
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XP_011535371.1:p.Ala632Ser
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XM_011537070.1:c.1837G>T
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XP_011535372.1:p.Ala613Ser
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XM_011537071.1:c.1804G>T
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XP_011535373.1:p.Ala602Ser
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XM_011537072.1:c.1783G>T
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XP_011535374.1:p.Ala595Ser
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XM_011537073.1:c.1576G>T
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XP_011535375.1:p.Ala526Ser
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XM_011537074.1:c.1576G>T
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XP_011535376.1:p.Ala526Ser
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XM_005267991.3:c.1990G>T
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XP_005268048.2:p.Ala664Ser
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XM_005267992.3:c.1984G>T
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XP_005268049.2:p.Ala662Ser
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XM_011537067.2:c.1933G>T
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XP_011535369.1:p.Ala645Ser
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XM_011537069.2:c.1981G>T
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XP_011535371.2:p.Ala661Ser
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XM_011537070.2:c.1837G>T
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XP_011535372.1:p.Ala613Ser
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XM_011537071.2:c.1891G>T
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XP_011535373.2:p.Ala631Ser
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XM_011537072.2:c.1783G>T
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XP_011535374.1:p.Ala595Ser
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XM_017021582.1:c.2041G>T
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XP_016877071.1:p.Ala681Ser
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XM_017021583.1:c.2032G>T
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XP_016877072.1:p.Ala678Ser
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XM_017021584.1:c.1951G>T
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XP_016877073.1:p.Ala651Ser
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XM_017021585.1:c.1900G>T
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XP_016877074.1:p.Ala634Ser
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XM_017021586.1:c.1576G>T
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XP_016877075.1:p.Ala526Ser
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XM_017021587.1:c.1576G>T
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XP_016877076.1:p.Ala526Ser
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XM_017021588.1:c.1576G>T
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XP_016877077.1:p.Ala526Ser
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NM_001164749.2:c.1882G>T
MANE Select
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NP_001158221.1:p.Ala628Ser
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NM_001165893.2:c.1792G>T
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NP_001159365.1:p.Ala598Ser
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NM_022123.3:c.1786G>T
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NP_071406.1:p.Ala596Ser
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NM_173159.3:c.1843G>T
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NP_775182.1:p.Ala615Ser
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NM_001394988.1:c.1837G>T
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NP_001381917.1:p.Ala613Ser
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NM_001394989.1:c.1783G>T
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NP_001381918.1:p.Ala595Ser
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