ENST00000371757.7:c.1317C>A
MANE Select
|
ENSP00000360822.2:p.Asp439Glu
|
|
ENST00000636003.1:c.7C>A
|
|
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ENST00000636995.1:n.44C>A
|
|
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ENST00000637798.1:n.56C>A
|
|
|
ENST00000674572.1:c.1158C>A
|
ENSP00000501742.1:p.Asp386Glu
|
|
ENST00000675090.1:c.1065C>A
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ENSP00000501833.1:p.Asp355Glu
|
|
ENST00000675399.1:c.1065C>A
|
ENSP00000501932.1:p.Asp355Glu
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|
ENST00000676421.1:c.1074C>A
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ENSP00000502322.1:p.Asp358Glu
|
|
ENST00000263604.5:c.1218C>A
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ENSP00000263604.4:p.Asp406Glu
|
|
ENST00000371757.6:c.1317C>A
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ENSP00000360822.2:p.Asp439Glu
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|
ENST00000460750.5:c.*927C>A
|
ENSP00000418777.1:n.*927C>A
|
|
ENST00000486577.6:c.1200C>A
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ENSP00000417578.3:p.Asp400Glu
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|
ENST00000487664.5:c.1317C>A
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ENSP00000417851.2:p.Asp439Glu
|
|
ENST00000488444.6:c.1260C>A
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ENSP00000419007.3:p.Asp420Glu
|
|
ENST00000490355.6:c.1260C>A
|
ENSP00000418003.3:p.Asp420Glu
|
|
ENST00000490363.3:n.1136C>A
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|
|
ENST00000491806.6:c.1260C>A
|
ENSP00000419086.3:p.Asp420Glu
|
|
ENST00000628528.2:c.1182C>A
|
ENSP00000486374.1:p.Asp394Glu
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|
ENST00000630792.2:c.1158C>A
|
ENSP00000486486.1:p.Asp386Glu
|
|
ENST00000631073.2:c.1260C>A
|
ENSP00000486130.1:p.Asp420Glu
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|
NM_001272003.1:c.1182C>A
|
NP_001258932.1:p.Asp394Glu
|
|
NM_020822.2:c.1317C>A
|
NP_065873.2:p.Asp439Glu
|
|
XM_011518877.1:c.1452C>A
|
XP_011517179.1:p.Asp484Glu
|
|
XM_011518878.1:c.1461C>A
|
XP_011517180.1:p.Asp487Glu
|
|
XM_011518879.1:c.1452C>A
|
XP_011517181.1:p.Asp484Glu
|
|
XM_011518880.1:c.1218C>A
|
XP_011517182.1:p.Asp406Glu
|
|
XM_011518881.1:c.807C>A
|
XP_011517183.1:p.Asp269Glu
|
|
XM_011518877.3:c.1452C>A
|
XP_011517179.1:p.Asp484Glu
|
|
XM_011518878.3:c.1461C>A
|
XP_011517180.1:p.Asp487Glu
|
|
XM_011518879.3:c.1452C>A
|
XP_011517181.1:p.Asp484Glu
|
|
XM_011518881.3:c.807C>A
|
XP_011517183.1:p.Asp269Glu
|
|
XM_017014931.1:c.1251C>A
|
XP_016870420.1:p.Asp417Glu
|
|
XM_017014932.1:c.1074C>A
|
XP_016870421.1:p.Asp358Glu
|
|
XM_017014933.1:c.807C>A
|
XP_016870422.1:p.Asp269Glu
|
|
XM_024447617.1:c.807C>A
|
XP_024303385.1:p.Asp269Glu
|
|
XM_024447618.1:c.807C>A
|
XP_024303386.1:p.Asp269Glu
|
|
NM_020822.3:c.1317C>A
MANE Select
|
NP_065873.2:p.Asp439Glu
|
|
NM_001272003.2:c.1182C>A
|
NP_001258932.1:p.Asp394Glu
|
|