ENST00000526209.2:c.304A>C
|
|
|
ENST00000681974.1:n.1006A>C
|
|
|
ENST00000682693.1:n.1968A>C
|
|
|
ENST00000682886.1:n.504A>C
|
|
|
ENST00000683543.2:c.16382A>C
|
ENSP00000506726.1:p.Glu5461Ala
|
|
ENST00000683988.1:c.305A>C
|
ENSP00000506939.1:p.Glu102Ala
|
|
ENST00000684428.1:c.869A>C
|
ENSP00000507433.1:p.Glu290Ala
|
|
ENST00000684755.1:n.917A>C
|
|
|
ENST00000685024.1:c.1488A>C
|
|
|
ENST00000685166.1:c.16343A>C
|
ENSP00000509386.1:p.Glu5448Ala
|
|
ENST00000688411.1:c.811A>C
|
ENSP00000510146.1:n.811A>C
|
|
ENST00000691932.1:c.335A>C
|
ENSP00000509037.1:p.Glu112Ala
|
|
ENST00000692637.1:c.16331A>C
|
ENSP00000509666.1:p.Glu5444Ala
|
|
ENST00000301067.12:c.16334A>C
MANE Select
|
ENSP00000301067.7:p.Glu5445Ala
|
|
ENST00000301067.11:c.16334A>C
|
ENSP00000301067.7:p.Glu5445Ala
|
|
ENST00000526209.1:c.377A>C
|
ENSP00000435714.1:p.Glu126Ala
|
|
NM_003482.3:c.16334A>C
|
NP_003473.3:p.Glu5445Ala
|
|
XM_005269162.3:c.16334A>C
|
XP_005269219.1:p.Glu5445Ala
|
|
XM_006719614.2:c.16343A>C
|
XP_006719677.1:p.Glu5448Ala
|
|
XM_006719616.2:c.16331A>C
|
XP_006719679.1:p.Glu5444Ala
|
|
XM_011538770.1:c.16391A>C
|
XP_011537072.1:p.Glu5464Ala
|
|
XM_011538771.1:c.16388A>C
|
XP_011537073.1:p.Glu5463Ala
|
|
XM_011538772.1:c.16382A>C
|
XP_011537074.1:p.Glu5461Ala
|
|
XM_011538773.1:c.16379A>C
|
XP_011537075.1:p.Glu5460Ala
|
|
XM_011538774.1:c.16370A>C
|
XP_011537076.1:p.Glu5457Ala
|
|
XM_011538775.1:c.16325A>C
|
XP_011537077.1:p.Glu5442Ala
|
|
XM_011538776.1:c.16298A>C
|
XP_011537078.1:p.Glu5433Ala
|
|
XM_005269162.4:c.16334A>C
|
XP_005269219.1:p.Glu5445Ala
|
|
XM_006719614.4:c.16343A>C
|
XP_006719677.1:p.Glu5448Ala
|
|
XM_006719616.3:c.16331A>C
|
XP_006719679.1:p.Glu5444Ala
|
|
XM_011538770.2:c.16391A>C
|
XP_011537072.1:p.Glu5464Ala
|
|
XM_011538771.2:c.16388A>C
|
XP_011537073.1:p.Glu5463Ala
|
|
XM_011538772.2:c.16382A>C
|
XP_011537074.1:p.Glu5461Ala
|
|
XM_011538773.2:c.16379A>C
|
XP_011537075.1:p.Glu5460Ala
|
|
XM_011538774.2:c.16370A>C
|
XP_011537076.1:p.Glu5457Ala
|
|
XM_011538776.2:c.16298A>C
|
XP_011537078.1:p.Glu5433Ala
|
|
XR_001748874.1:n.16511A>C
|
|
|
NM_003482.4:c.16334A>C
MANE Select
|
NP_003473.3:p.Glu5445Ala
|
|