ENST00000706989.1:c.1992G>A
|
ENSP00000516702.1:p.Gln664=
|
|
ENST00000359125.7:c.1938G>A
MANE Select
|
ENSP00000352035.2:p.Gln646=
|
|
ENST00000637193.1:c.1335G>A
|
ENSP00000490734.1:p.Gln445=
|
|
ENST00000637338.1:n.95G>A
|
|
|
ENST00000344462.8:c.1845G>A
|
ENSP00000339611.4:p.Gln615=
|
|
ENST00000357249.6:c.1506G>A
|
ENSP00000349789.3:p.Gln502=
|
|
ENST00000359125.6:c.1938G>A
|
ENSP00000352035.2:p.Gln646=
|
|
ENST00000360480.7:c.1854G>A
|
ENSP00000353668.3:p.Gln618=
|
|
ENST00000370224.5:c.1962G>A
|
ENSP00000359244.2:p.Gln654=
|
|
ENST00000625514.2:c.1926G>A
|
ENSP00000486040.1:p.Gln642=
|
|
ENST00000626839.2:c.1884G>A
|
ENSP00000486706.1:p.Gln628=
|
|
ENST00000629241.2:c.1854G>A
|
ENSP00000487142.1:p.Gln618=
|
|
ENST00000629676.2:c.1679+6125G>A
|
ENSP00000486194.1:n.1679+6125G>A
|
|
NM_004518.4:c.1854G>A
|
NP_004509.2:p.Gln618=
|
|
NM_172106.1:c.1884G>A
|
NP_742104.1:p.Gln628=
|
|
NM_172107.2:c.1938G>A
|
NP_742105.1:p.Gln646=
|
|
NM_172108.3:c.1845G>A
|
NP_742106.1:p.Gln615=
|
|
XM_006723787.1:c.1980G>A
|
XP_006723850.1:p.Gln660=
|
|
XM_011528807.1:c.2046G>A
|
XP_011527109.1:p.Gln682=
|
|
XM_011528808.1:c.2043G>A
|
XP_011527110.1:p.Gln681=
|
|
XM_011528809.1:c.2016G>A
|
XP_011527111.1:p.Gln672=
|
|
XM_011528810.1:c.1992G>A
|
XP_011527112.1:p.Gln664=
|
|
XM_011528811.1:c.1962G>A
|
XP_011527113.1:p.Gln654=
|
|
XM_011528812.1:c.1935G>A
|
XP_011527114.1:p.Gln645=
|
|
XM_011528813.1:c.1920G>A
|
XP_011527115.1:p.Gln640=
|
|
XM_011528814.1:c.1527G>A
|
XP_011527116.1:p.Gln509=
|
|
NM_004518.5:c.1854G>A
|
NP_004509.2:p.Gln618=
|
|
NM_172106.2:c.1884G>A
|
NP_742104.1:p.Gln628=
|
|
NM_172107.3:c.1938G>A
|
NP_742105.1:p.Gln646=
|
|
NM_172108.4:c.1845G>A
|
NP_742106.1:p.Gln615=
|
|
XM_011528810.2:c.1992G>A
|
XP_011527112.1:p.Gln664=
|
|
XM_011528811.2:c.1962G>A
|
XP_011527113.1:p.Gln654=
|
|
XM_017027841.2:c.1989G>A
|
XP_016883330.1:p.Gln663=
|
|
XM_017027842.2:c.1926G>A
|
XP_016883331.1:p.Gln642=
|
|
XM_017027843.1:c.1923G>A
|
XP_016883332.1:p.Gln641=
|
|
XM_017027844.2:c.1881G>A
|
XP_016883333.1:p.Gln627=
|
|
XM_017027845.1:c.954G>A
|
XP_016883334.1:p.Gln318=
|
|
NM_004518.6:c.1854G>A
|
NP_004509.2:p.Gln618=
|
|
NM_172106.3:c.1884G>A
|
NP_742104.1:p.Gln628=
|
|
NM_172107.4:c.1938G>A
MANE Select
|
NP_742105.1:p.Gln646=
|
|
NM_172108.5:c.1845G>A
|
NP_742106.1:p.Gln615=
|
|
NM_001382235.1:c.1992G>A
|
NP_001369164.1:p.Gln664=
|
|