ENST00000706989.1:c.2361G>C
|
ENSP00000516702.1:p.Glu787Asp
|
|
ENST00000359125.7:c.2307G>C
MANE Select
|
ENSP00000352035.2:p.Glu769Asp
|
|
ENST00000637193.1:c.1704G>C
|
ENSP00000490734.1:p.Glu568Asp
|
|
ENST00000344462.8:c.2214G>C
|
ENSP00000339611.4:p.Glu738Asp
|
|
ENST00000357249.6:c.1875G>C
|
ENSP00000349789.3:p.Glu625Asp
|
|
ENST00000359125.6:c.2307G>C
|
ENSP00000352035.2:p.Glu769Asp
|
|
ENST00000360480.7:c.2223G>C
|
ENSP00000353668.3:p.Glu741Asp
|
|
ENST00000370224.5:c.2241+90G>C
|
ENSP00000359244.2:n.2241+90G>C
|
|
ENST00000625514.2:c.2205+90G>C
|
ENSP00000486040.1:n.2205+90G>C
|
|
ENST00000626839.2:c.2253G>C
|
ENSP00000486706.1:p.Glu751Asp
|
|
ENST00000629241.2:c.2133+90G>C
|
ENSP00000487142.1:n.2133+90G>C
|
|
ENST00000629676.2:c.1680-6113G>C
|
ENSP00000486194.1:n.1680-6113G>C
|
|
NM_004518.4:c.2223G>C
|
NP_004509.2:p.Glu741Asp
|
|
NM_172106.1:c.2253G>C
|
NP_742104.1:p.Glu751Asp
|
|
NM_172107.2:c.2307G>C
|
NP_742105.1:p.Glu769Asp
|
|
NM_172108.3:c.2214G>C
|
NP_742106.1:p.Glu738Asp
|
|
XM_006723787.1:c.2349G>C
|
XP_006723850.1:p.Glu783Asp
|
|
XM_011528807.1:c.2415G>C
|
XP_011527109.1:p.Glu805Asp
|
|
XM_011528808.1:c.2412G>C
|
XP_011527110.1:p.Glu804Asp
|
|
XM_011528809.1:c.2385G>C
|
XP_011527111.1:p.Glu795Asp
|
|
XM_011528810.1:c.2361G>C
|
XP_011527112.1:p.Glu787Asp
|
|
XM_011528811.1:c.2331G>C
|
XP_011527113.1:p.Glu777Asp
|
|
XM_011528812.1:c.2304G>C
|
XP_011527114.1:p.Glu768Asp
|
|
XM_011528813.1:c.2289G>C
|
XP_011527115.1:p.Glu763Asp
|
|
XM_011528814.1:c.1896G>C
|
XP_011527116.1:p.Glu632Asp
|
|
NM_004518.5:c.2223G>C
|
NP_004509.2:p.Glu741Asp
|
|
NM_172106.2:c.2253G>C
|
NP_742104.1:p.Glu751Asp
|
|
NM_172107.3:c.2307G>C
|
NP_742105.1:p.Glu769Asp
|
|
NM_172108.4:c.2214G>C
|
NP_742106.1:p.Glu738Asp
|
|
XM_011528810.2:c.2361G>C
|
XP_011527112.1:p.Glu787Asp
|
|
XM_011528811.2:c.2331G>C
|
XP_011527113.1:p.Glu777Asp
|
|
XM_017027841.2:c.2358G>C
|
XP_016883330.1:p.Glu786Asp
|
|
XM_017027842.2:c.2295G>C
|
XP_016883331.1:p.Glu765Asp
|
|
XM_017027843.1:c.2292G>C
|
XP_016883332.1:p.Glu764Asp
|
|
XM_017027844.2:c.2250G>C
|
XP_016883333.1:p.Glu750Asp
|
|
XM_017027845.1:c.1323G>C
|
XP_016883334.1:p.Glu441Asp
|
|
NM_004518.6:c.2223G>C
|
NP_004509.2:p.Glu741Asp
|
|
NM_172106.3:c.2253G>C
|
NP_742104.1:p.Glu751Asp
|
|
NM_172107.4:c.2307G>C
MANE Select
|
NP_742105.1:p.Glu769Asp
|
|
NM_172108.5:c.2214G>C
|
NP_742106.1:p.Glu738Asp
|
|
NM_001382235.1:c.2361G>C
|
NP_001369164.1:p.Glu787Asp
|
|