|
ENST00000707132.1:n.1961A>C
|
|
|
|
ENST00000707133.1:n.391A>C
|
|
|
|
ENST00000707134.1:n.660A>C
|
|
|
|
ENST00000346798.8:c.1994A>C
MANE Select
|
ENSP00000284981.4:p.Glu665Ala
|
|
|
ENST00000346798.7:c.1994A>C
|
ENSP00000284981.4:p.Glu665Ala
|
|
|
ENST00000348990.9:c.1769A>C
|
ENSP00000345463.5:p.Glu590Ala
|
|
|
ENST00000354192.7:c.1601A>C
|
ENSP00000346129.3:p.Glu534Ala
|
|
|
ENST00000357903.7:c.1937A>C
|
ENSP00000350578.3:p.Glu646Ala
|
|
|
ENST00000358918.7:c.1940A>C
|
ENSP00000351796.3:p.Glu647Ala
|
|
|
ENST00000359726.7:c.1664A>C
|
ENSP00000352760.4:p.Glu555Ala
|
|
|
ENST00000439274.6:c.1826A>C
|
ENSP00000398879.2:p.Glu609Ala
|
|
|
ENST00000440126.7:c.1922A>C
|
ENSP00000387483.2:p.Glu641Ala
|
|
|
ENST00000464867.1:n.341A>C
|
|
|
|
NM_000484.3:c.1994A>C
|
NP_000475.1:p.Glu665Ala
|
|
|
NM_001136016.3:c.1922A>C
|
NP_001129488.1:p.Glu641Ala
|
|
|
NM_001136129.2:c.1601A>C
|
NP_001129601.1:p.Glu534Ala
|
|
|
NM_001136130.2:c.1826A>C
|
NP_001129602.1:p.Glu609Ala
|
|
|
NM_001136131.2:c.1664A>C
|
NP_001129603.1:p.Glu555Ala
|
|
|
NM_001204301.1:c.1940A>C
|
NP_001191230.1:p.Glu647Ala
|
|
|
NM_001204302.1:c.1883A>C
|
NP_001191231.1:p.Glu628Ala
|
|
|
NM_001204303.1:c.1715A>C
|
NP_001191232.1:p.Glu572Ala
|
|
|
NM_201413.2:c.1937A>C
|
NP_958816.1:p.Glu646Ala
|
|
|
NM_201414.2:c.1769A>C
|
NP_958817.1:p.Glu590Ala
|
|
|
NM_000484.4:c.1994A>C
MANE Select
|
NP_000475.1:p.Glu665Ala
|
|
|
NM_001136129.3:c.1601A>C
|
NP_001129601.1:p.Glu534Ala
|
|
|
NM_001136130.3:c.1826A>C
|
NP_001129602.1:p.Glu609Ala
|
|
|
NM_001204301.2:c.1940A>C
|
NP_001191230.1:p.Glu647Ala
|
|
|
NM_001204302.2:c.1883A>C
|
NP_001191231.1:p.Glu628Ala
|
|
|
NM_001204303.2:c.1715A>C
|
NP_001191232.1:p.Glu572Ala
|
|
|
NM_201413.3:c.1937A>C
|
NP_958816.1:p.Glu646Ala
|
|
|
NM_201414.3:c.1769A>C
|
NP_958817.1:p.Glu590Ala
|
|
|
NM_001136131.3:c.1664A>C
|
NP_001129603.1:p.Glu555Ala
|
|
|
NM_001385253.1:c.1826A>C
|
NP_001372182.1:p.Glu609Ala
|
|
