ENST00000706989.1:c.2021A>C
|
ENSP00000516702.1:p.Glu674Ala
|
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ENST00000359125.7:c.1967A>C
MANE Select
|
ENSP00000352035.2:p.Glu656Ala
|
|
ENST00000637193.1:c.1364A>C
|
ENSP00000490734.1:p.Glu455Ala
|
|
ENST00000344462.8:c.1874A>C
|
ENSP00000339611.4:p.Glu625Ala
|
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ENST00000357249.6:c.1535A>C
|
ENSP00000349789.3:p.Glu512Ala
|
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ENST00000359125.6:c.1967A>C
|
ENSP00000352035.2:p.Glu656Ala
|
|
ENST00000360480.7:c.1883A>C
|
ENSP00000353668.3:p.Glu628Ala
|
|
ENST00000370224.5:c.1991A>C
|
ENSP00000359244.2:p.Glu664Ala
|
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ENST00000625514.2:c.1955A>C
|
ENSP00000486040.1:p.Glu652Ala
|
|
ENST00000626839.2:c.1913A>C
|
ENSP00000486706.1:p.Glu638Ala
|
|
ENST00000629241.2:c.1883A>C
|
ENSP00000487142.1:p.Glu628Ala
|
|
ENST00000629676.2:c.1679+6154A>C
|
ENSP00000486194.1:n.1679+6154A>C
|
|
NM_004518.4:c.1883A>C
|
NP_004509.2:p.Glu628Ala
|
|
NM_172106.1:c.1913A>C
|
NP_742104.1:p.Glu638Ala
|
|
NM_172107.2:c.1967A>C
|
NP_742105.1:p.Glu656Ala
|
|
NM_172108.3:c.1874A>C
|
NP_742106.1:p.Glu625Ala
|
|
XM_006723787.1:c.2009A>C
|
XP_006723850.1:p.Glu670Ala
|
|
XM_011528807.1:c.2075A>C
|
XP_011527109.1:p.Glu692Ala
|
|
XM_011528808.1:c.2072A>C
|
XP_011527110.1:p.Glu691Ala
|
|
XM_011528809.1:c.2045A>C
|
XP_011527111.1:p.Glu682Ala
|
|
XM_011528810.1:c.2021A>C
|
XP_011527112.1:p.Glu674Ala
|
|
XM_011528811.1:c.1991A>C
|
XP_011527113.1:p.Glu664Ala
|
|
XM_011528812.1:c.1964A>C
|
XP_011527114.1:p.Glu655Ala
|
|
XM_011528813.1:c.1949A>C
|
XP_011527115.1:p.Glu650Ala
|
|
XM_011528814.1:c.1556A>C
|
XP_011527116.1:p.Glu519Ala
|
|
NM_004518.5:c.1883A>C
|
NP_004509.2:p.Glu628Ala
|
|
NM_172106.2:c.1913A>C
|
NP_742104.1:p.Glu638Ala
|
|
NM_172107.3:c.1967A>C
|
NP_742105.1:p.Glu656Ala
|
|
NM_172108.4:c.1874A>C
|
NP_742106.1:p.Glu625Ala
|
|
XM_011528810.2:c.2021A>C
|
XP_011527112.1:p.Glu674Ala
|
|
XM_011528811.2:c.1991A>C
|
XP_011527113.1:p.Glu664Ala
|
|
XM_017027841.2:c.2018A>C
|
XP_016883330.1:p.Glu673Ala
|
|
XM_017027842.2:c.1955A>C
|
XP_016883331.1:p.Glu652Ala
|
|
XM_017027843.1:c.1952A>C
|
XP_016883332.1:p.Glu651Ala
|
|
XM_017027844.2:c.1910A>C
|
XP_016883333.1:p.Glu637Ala
|
|
XM_017027845.1:c.983A>C
|
XP_016883334.1:p.Glu328Ala
|
|
NM_004518.6:c.1883A>C
|
NP_004509.2:p.Glu628Ala
|
|
NM_172106.3:c.1913A>C
|
NP_742104.1:p.Glu638Ala
|
|
NM_172107.4:c.1967A>C
MANE Select
|
NP_742105.1:p.Glu656Ala
|
|
NM_172108.5:c.1874A>C
|
NP_742106.1:p.Glu625Ala
|
|
NM_001382235.1:c.2021A>C
|
NP_001369164.1:p.Glu674Ala
|
|