ENST00000706989.1:c.2489A>G
|
ENSP00000516702.1:p.Glu830Gly
|
|
ENST00000359125.7:c.2435A>G
MANE Select
|
ENSP00000352035.2:p.Glu812Gly
|
|
ENST00000637193.1:c.1832A>G
|
ENSP00000490734.1:p.Glu611Gly
|
|
ENST00000344462.8:c.2342A>G
|
ENSP00000339611.4:p.Glu781Gly
|
|
ENST00000357249.6:c.2003A>G
|
ENSP00000349789.3:p.Glu668Gly
|
|
ENST00000359125.6:c.2435A>G
|
ENSP00000352035.2:p.Glu812Gly
|
|
ENST00000360480.7:c.2351A>G
|
ENSP00000353668.3:p.Glu784Gly
|
|
ENST00000370224.5:c.2241+218A>G
|
ENSP00000359244.2:n.2241+218A>G
|
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ENST00000625514.2:c.2205+218A>G
|
ENSP00000486040.1:n.2205+218A>G
|
|
ENST00000626839.2:c.2381A>G
|
ENSP00000486706.1:p.Glu794Gly
|
|
ENST00000629241.2:c.2133+218A>G
|
ENSP00000487142.1:n.2133+218A>G
|
|
ENST00000629676.2:c.1680-5985A>G
|
ENSP00000486194.1:n.1680-5985A>G
|
|
NM_004518.4:c.2351A>G
|
NP_004509.2:p.Glu784Gly
|
|
NM_172106.1:c.2381A>G
|
NP_742104.1:p.Glu794Gly
|
|
NM_172107.2:c.2435A>G
|
NP_742105.1:p.Glu812Gly
|
|
NM_172108.3:c.2342A>G
|
NP_742106.1:p.Glu781Gly
|
|
XM_006723787.1:c.2477A>G
|
XP_006723850.1:p.Glu826Gly
|
|
XM_011528807.1:c.2543A>G
|
XP_011527109.1:p.Glu848Gly
|
|
XM_011528808.1:c.2540A>G
|
XP_011527110.1:p.Glu847Gly
|
|
XM_011528809.1:c.2513A>G
|
XP_011527111.1:p.Glu838Gly
|
|
XM_011528810.1:c.2489A>G
|
XP_011527112.1:p.Glu830Gly
|
|
XM_011528811.1:c.2459A>G
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XP_011527113.1:p.Glu820Gly
|
|
XM_011528812.1:c.2432A>G
|
XP_011527114.1:p.Glu811Gly
|
|
XM_011528813.1:c.2417A>G
|
XP_011527115.1:p.Glu806Gly
|
|
XM_011528814.1:c.2024A>G
|
XP_011527116.1:p.Glu675Gly
|
|
NM_004518.5:c.2351A>G
|
NP_004509.2:p.Glu784Gly
|
|
NM_172106.2:c.2381A>G
|
NP_742104.1:p.Glu794Gly
|
|
NM_172107.3:c.2435A>G
|
NP_742105.1:p.Glu812Gly
|
|
NM_172108.4:c.2342A>G
|
NP_742106.1:p.Glu781Gly
|
|
XM_011528810.2:c.2489A>G
|
XP_011527112.1:p.Glu830Gly
|
|
XM_011528811.2:c.2459A>G
|
XP_011527113.1:p.Glu820Gly
|
|
XM_017027841.2:c.2486A>G
|
XP_016883330.1:p.Glu829Gly
|
|
XM_017027842.2:c.2423A>G
|
XP_016883331.1:p.Glu808Gly
|
|
XM_017027843.1:c.2420A>G
|
XP_016883332.1:p.Glu807Gly
|
|
XM_017027844.2:c.2378A>G
|
XP_016883333.1:p.Glu793Gly
|
|
XM_017027845.1:c.1451A>G
|
XP_016883334.1:p.Glu484Gly
|
|
NM_004518.6:c.2351A>G
|
NP_004509.2:p.Glu784Gly
|
|
NM_172106.3:c.2381A>G
|
NP_742104.1:p.Glu794Gly
|
|
NM_172107.4:c.2435A>G
MANE Select
|
NP_742105.1:p.Glu812Gly
|
|
NM_172108.5:c.2342A>G
|
NP_742106.1:p.Glu781Gly
|
|
NM_001382235.1:c.2489A>G
|
NP_001369164.1:p.Glu830Gly
|
|