ENST00000324602.12:c.1757A>T
MANE Select
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ENSP00000315997.7:p.Glu586Val
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ENST00000324602.11:c.1757A>T
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ENSP00000315997.7:p.Glu586Val
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ENST00000396315.5:c.1757A>T
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ENSP00000379608.1:p.Glu586Val
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ENST00000396317.5:c.1703A>T
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ENSP00000379610.1:p.Glu568Val
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ENST00000396327.7:c.1754A>T
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ENSP00000379618.3:p.Glu585Val
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ENST00000396331.5:c.1751A>T
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ENSP00000379622.1:p.Glu584Val
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ENST00000396332.8:c.1754A>T
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ENSP00000379623.4:p.Glu585Val
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ENST00000421584.5:c.1675A>T
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ENSP00000410165.1:n.1675A>T
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ENST00000427581.6:c.1904A>T
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ENSP00000395004.2:p.Glu635Val
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ENST00000462628.5:n.1535A>T
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NM_001081637.2:c.1757A>T
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NP_001075106.2:p.Glu586Val
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NM_001081638.3:c.1754A>T
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NP_001075107.2:p.Glu585Val
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NM_001081639.3:c.1754A>T
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NP_001075108.2:p.Glu585Val
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NM_001278398.2:c.1703A>T
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NP_001265327.2:p.Glu568Val
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NM_006669.6:c.1751A>T
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NP_006660.4:p.Glu584Val
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NR_103518.2:n.1840A>T
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XM_011526331.1:c.1787A>T
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XP_011524633.1:p.Glu596Val
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XM_011526332.1:c.1784A>T
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XP_011524634.1:p.Glu595Val
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XM_011526333.1:c.1784A>T
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XP_011524635.1:p.Glu595Val
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XM_011526334.1:c.1808A>T
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XP_011524636.1:p.Glu603Val
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XM_011526335.1:c.1684-135A>T
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XP_011524637.1:n.1684-135A>T
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XM_011526336.1:c.1651-135A>T
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XP_011524638.1:n.1651-135A>T
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XM_011526339.1:c.1751A>T
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XP_011524641.1:p.Glu584Val
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XM_011526331.2:c.1787A>T
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XP_011524633.1:p.Glu596Val
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XM_011526332.3:c.1784A>T
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XP_011524634.1:p.Glu595Val
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XM_011526335.2:c.1684-135A>T
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XP_011524637.1:n.1684-135A>T
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XM_011526336.2:c.1651-135A>T
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XP_011524638.1:n.1651-135A>T
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XM_017026182.2:c.1784A>T
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XP_016881671.1:p.Glu595Val
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XM_017026183.2:c.1781A>T
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XP_016881672.1:p.Glu594Val
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XM_017026184.2:c.1781A>T
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XP_016881673.1:p.Glu594Val
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XM_017026185.1:c.1751A>T
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XP_016881674.1:p.Glu584Val
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XM_017026186.1:c.1808A>T
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XP_016881675.1:p.Glu603Val
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XM_017026187.1:c.1808A>T
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XP_016881676.1:p.Glu603Val
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XM_017026188.1:c.1805A>T
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XP_016881677.1:p.Glu602Val
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XM_017026189.1:c.1805A>T
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XP_016881678.1:p.Glu602Val
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XM_017026190.1:c.1802A>T
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XP_016881679.1:p.Glu601Val
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XM_017026191.1:c.1654-135A>T
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XP_016881680.1:n.1654-135A>T
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XR_001753590.2:n.2004A>T
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XR_001753591.1:n.2009A>T
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XR_002958244.1:n.2001A>T
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NM_001081637.3:c.1757A>T
MANE Select
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NP_001075106.2:p.Glu586Val
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NM_001081638.4:c.1754A>T
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NP_001075107.2:p.Glu585Val
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NM_001081639.4:c.1754A>T
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NP_001075108.2:p.Glu585Val
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NM_001388355.1:c.1754A>T
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NP_001375284.1:p.Glu585Val
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NM_001388356.1:c.1754A>T
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NP_001375285.1:p.Glu585Val
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NM_001388357.1:c.1754A>T
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NP_001375286.1:p.Glu585Val
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NM_001388358.1:c.1757A>T
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NP_001375287.1:p.Glu586Val
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NM_006669.7:c.1751A>T
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NP_006660.4:p.Glu584Val
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