ENST00000706989.1:c.1955A>T
|
ENSP00000516702.1:p.Glu652Val
|
|
ENST00000359125.7:c.1901A>T
MANE Select
|
ENSP00000352035.2:p.Glu634Val
|
|
ENST00000637193.1:c.1298A>T
|
ENSP00000490734.1:p.Glu433Val
|
|
ENST00000637338.1:n.58A>T
|
|
|
ENST00000344462.8:c.1808A>T
|
ENSP00000339611.4:p.Glu603Val
|
|
ENST00000357249.6:c.1469A>T
|
ENSP00000349789.3:p.Glu490Val
|
|
ENST00000359125.6:c.1901A>T
|
ENSP00000352035.2:p.Glu634Val
|
|
ENST00000360480.7:c.1817A>T
|
ENSP00000353668.3:p.Glu606Val
|
|
ENST00000370224.5:c.1925A>T
|
ENSP00000359244.2:p.Glu642Val
|
|
ENST00000625514.2:c.1889A>T
|
ENSP00000486040.1:p.Glu630Val
|
|
ENST00000626839.2:c.1847A>T
|
ENSP00000486706.1:p.Glu616Val
|
|
ENST00000629241.2:c.1817A>T
|
ENSP00000487142.1:p.Glu606Val
|
|
ENST00000629676.2:c.1679+6088A>T
|
ENSP00000486194.1:n.1679+6088A>T
|
|
NM_004518.4:c.1817A>T
|
NP_004509.2:p.Glu606Val
|
|
NM_172106.1:c.1847A>T
|
NP_742104.1:p.Glu616Val
|
|
NM_172107.2:c.1901A>T
|
NP_742105.1:p.Glu634Val
|
|
NM_172108.3:c.1808A>T
|
NP_742106.1:p.Glu603Val
|
|
XM_006723787.1:c.1943A>T
|
XP_006723850.1:p.Glu648Val
|
|
XM_011528807.1:c.2009A>T
|
XP_011527109.1:p.Glu670Val
|
|
XM_011528808.1:c.2006A>T
|
XP_011527110.1:p.Glu669Val
|
|
XM_011528809.1:c.1979A>T
|
XP_011527111.1:p.Glu660Val
|
|
XM_011528810.1:c.1955A>T
|
XP_011527112.1:p.Glu652Val
|
|
XM_011528811.1:c.1925A>T
|
XP_011527113.1:p.Glu642Val
|
|
XM_011528812.1:c.1898A>T
|
XP_011527114.1:p.Glu633Val
|
|
XM_011528813.1:c.1883A>T
|
XP_011527115.1:p.Glu628Val
|
|
XM_011528814.1:c.1490A>T
|
XP_011527116.1:p.Glu497Val
|
|
NM_004518.5:c.1817A>T
|
NP_004509.2:p.Glu606Val
|
|
NM_172106.2:c.1847A>T
|
NP_742104.1:p.Glu616Val
|
|
NM_172107.3:c.1901A>T
|
NP_742105.1:p.Glu634Val
|
|
NM_172108.4:c.1808A>T
|
NP_742106.1:p.Glu603Val
|
|
XM_011528810.2:c.1955A>T
|
XP_011527112.1:p.Glu652Val
|
|
XM_011528811.2:c.1925A>T
|
XP_011527113.1:p.Glu642Val
|
|
XM_017027841.2:c.1952A>T
|
XP_016883330.1:p.Glu651Val
|
|
XM_017027842.2:c.1889A>T
|
XP_016883331.1:p.Glu630Val
|
|
XM_017027843.1:c.1886A>T
|
XP_016883332.1:p.Glu629Val
|
|
XM_017027844.2:c.1844A>T
|
XP_016883333.1:p.Glu615Val
|
|
XM_017027845.1:c.917A>T
|
XP_016883334.1:p.Glu306Val
|
|
NM_004518.6:c.1817A>T
|
NP_004509.2:p.Glu606Val
|
|
NM_172106.3:c.1847A>T
|
NP_742104.1:p.Glu616Val
|
|
NM_172107.4:c.1901A>T
MANE Select
|
NP_742105.1:p.Glu634Val
|
|
NM_172108.5:c.1808A>T
|
NP_742106.1:p.Glu603Val
|
|
NM_001382235.1:c.1955A>T
|
NP_001369164.1:p.Glu652Val
|
|