|
ENST00000707132.1:n.1962G>T
|
|
|
|
ENST00000707133.1:n.392G>T
|
|
|
|
ENST00000707134.1:n.661G>T
|
|
|
|
ENST00000346798.8:c.1995G>T
MANE Select
|
ENSP00000284981.4:p.Glu665Asp
|
|
|
ENST00000346798.7:c.1995G>T
|
ENSP00000284981.4:p.Glu665Asp
|
|
|
ENST00000348990.9:c.1770G>T
|
ENSP00000345463.5:p.Glu590Asp
|
|
|
ENST00000354192.7:c.1602G>T
|
ENSP00000346129.3:p.Glu534Asp
|
|
|
ENST00000357903.7:c.1938G>T
|
ENSP00000350578.3:p.Glu646Asp
|
|
|
ENST00000358918.7:c.1941G>T
|
ENSP00000351796.3:p.Glu647Asp
|
|
|
ENST00000359726.7:c.1665G>T
|
ENSP00000352760.4:p.Glu555Asp
|
|
|
ENST00000439274.6:c.1827G>T
|
ENSP00000398879.2:p.Glu609Asp
|
|
|
ENST00000440126.7:c.1923G>T
|
ENSP00000387483.2:p.Glu641Asp
|
|
|
ENST00000464867.1:n.342G>T
|
|
|
|
NM_000484.3:c.1995G>T
|
NP_000475.1:p.Glu665Asp
|
|
|
NM_001136016.3:c.1923G>T
|
NP_001129488.1:p.Glu641Asp
|
|
|
NM_001136129.2:c.1602G>T
|
NP_001129601.1:p.Glu534Asp
|
|
|
NM_001136130.2:c.1827G>T
|
NP_001129602.1:p.Glu609Asp
|
|
|
NM_001136131.2:c.1665G>T
|
NP_001129603.1:p.Glu555Asp
|
|
|
NM_001204301.1:c.1941G>T
|
NP_001191230.1:p.Glu647Asp
|
|
|
NM_001204302.1:c.1884G>T
|
NP_001191231.1:p.Glu628Asp
|
|
|
NM_001204303.1:c.1716G>T
|
NP_001191232.1:p.Glu572Asp
|
|
|
NM_201413.2:c.1938G>T
|
NP_958816.1:p.Glu646Asp
|
|
|
NM_201414.2:c.1770G>T
|
NP_958817.1:p.Glu590Asp
|
|
|
NM_000484.4:c.1995G>T
MANE Select
|
NP_000475.1:p.Glu665Asp
|
|
|
NM_001136129.3:c.1602G>T
|
NP_001129601.1:p.Glu534Asp
|
|
|
NM_001136130.3:c.1827G>T
|
NP_001129602.1:p.Glu609Asp
|
|
|
NM_001204301.2:c.1941G>T
|
NP_001191230.1:p.Glu647Asp
|
|
|
NM_001204302.2:c.1884G>T
|
NP_001191231.1:p.Glu628Asp
|
|
|
NM_001204303.2:c.1716G>T
|
NP_001191232.1:p.Glu572Asp
|
|
|
NM_201413.3:c.1938G>T
|
NP_958816.1:p.Glu646Asp
|
|
|
NM_201414.3:c.1770G>T
|
NP_958817.1:p.Glu590Asp
|
|
|
NM_001136131.3:c.1665G>T
|
NP_001129603.1:p.Glu555Asp
|
|
|
NM_001385253.1:c.1827G>T
|
NP_001372182.1:p.Glu609Asp
|
|
