ENST00000356141.9:c.1895A>C
MANE Select
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ENSP00000348460.4:p.Glu632Ala
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ENST00000551634.6:c.1904A>C
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ENSP00000448373.2:p.Glu635Ala
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ENST00000680362.1:c.1795A>C
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ENST00000681323.1:c.793+2621A>C
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ENST00000346562.6:c.1799A>C
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ENSP00000319610.5:p.Glu600Ala
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ENST00000356141.8:c.1895A>C
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ENSP00000348460.4:p.Glu632Ala
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ENST00000357798.9:c.1856A>C
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ENSP00000350446.5:p.Glu619Ala
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ENST00000548645.5:c.1805A>C
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ENSP00000448916.1:p.Glu602Ala
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ENST00000551492.5:c.1910A>C
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ENSP00000450392.1:p.Glu637Ala
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ENST00000551634.5:c.1817A>C
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ENSP00000448373.1:p.Glu606Ala
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NM_001164749.1:c.1895A>C
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NP_001158221.1:p.Glu632Ala
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NM_001165893.1:c.1805A>C
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NP_001159365.1:p.Glu602Ala
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NM_022123.2:c.1799A>C
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NP_071406.1:p.Glu600Ala
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NM_173159.2:c.1856A>C
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NP_775182.1:p.Glu619Ala
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XM_005267991.2:c.1916A>C
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XP_005268048.1:p.Glu639Ala
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XM_005267992.2:c.1910A>C
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XP_005268049.1:p.Glu637Ala
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XM_005267993.2:c.1856A>C
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XP_005268050.1:p.Glu619Ala
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XM_011537067.1:c.1946A>C
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XP_011535369.1:p.Glu649Ala
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XM_011537068.1:c.1937A>C
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XP_011535370.1:p.Glu646Ala
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XM_011537069.1:c.1907A>C
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XP_011535371.1:p.Glu636Ala
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XM_011537070.1:c.1850A>C
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XP_011535372.1:p.Glu617Ala
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XM_011537071.1:c.1817A>C
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XP_011535373.1:p.Glu606Ala
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XM_011537072.1:c.1796A>C
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XP_011535374.1:p.Glu599Ala
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XM_011537073.1:c.1589A>C
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XP_011535375.1:p.Glu530Ala
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XM_011537074.1:c.1589A>C
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XP_011535376.1:p.Glu530Ala
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XM_005267991.3:c.2003A>C
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XP_005268048.2:p.Glu668Ala
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XM_005267992.3:c.1997A>C
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XP_005268049.2:p.Glu666Ala
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XM_011537067.2:c.1946A>C
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XP_011535369.1:p.Glu649Ala
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XM_011537069.2:c.1994A>C
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XP_011535371.2:p.Glu665Ala
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XM_011537070.2:c.1850A>C
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XP_011535372.1:p.Glu617Ala
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XM_011537071.2:c.1904A>C
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XP_011535373.2:p.Glu635Ala
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XM_011537072.2:c.1796A>C
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XP_011535374.1:p.Glu599Ala
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XM_017021582.1:c.2054A>C
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XP_016877071.1:p.Glu685Ala
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XM_017021583.1:c.2045A>C
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XP_016877072.1:p.Glu682Ala
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XM_017021584.1:c.1964A>C
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XP_016877073.1:p.Glu655Ala
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XM_017021585.1:c.1913A>C
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XP_016877074.1:p.Glu638Ala
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XM_017021586.1:c.1589A>C
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XP_016877075.1:p.Glu530Ala
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XM_017021587.1:c.1589A>C
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XP_016877076.1:p.Glu530Ala
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XM_017021588.1:c.1589A>C
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XP_016877077.1:p.Glu530Ala
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NM_001164749.2:c.1895A>C
MANE Select
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NP_001158221.1:p.Glu632Ala
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NM_001165893.2:c.1805A>C
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NP_001159365.1:p.Glu602Ala
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NM_022123.3:c.1799A>C
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NP_071406.1:p.Glu600Ala
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NM_173159.3:c.1856A>C
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NP_775182.1:p.Glu619Ala
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NM_001394988.1:c.1850A>C
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NP_001381917.1:p.Glu617Ala
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NM_001394989.1:c.1796A>C
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NP_001381918.1:p.Glu599Ala
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