ENST00000706989.1:c.2392A>G
|
ENSP00000516702.1:p.Asn798Asp
|
|
ENST00000359125.7:c.2338A>G
MANE Select
|
ENSP00000352035.2:p.Asn780Asp
|
|
ENST00000637193.1:c.1735A>G
|
ENSP00000490734.1:p.Asn579Asp
|
|
ENST00000344462.8:c.2245A>G
|
ENSP00000339611.4:p.Asn749Asp
|
|
ENST00000357249.6:c.1906A>G
|
ENSP00000349789.3:p.Asn636Asp
|
|
ENST00000359125.6:c.2338A>G
|
ENSP00000352035.2:p.Asn780Asp
|
|
ENST00000360480.7:c.2254A>G
|
ENSP00000353668.3:p.Asn752Asp
|
|
ENST00000370224.5:c.2241+121A>G
|
ENSP00000359244.2:n.2241+121A>G
|
|
ENST00000625514.2:c.2205+121A>G
|
ENSP00000486040.1:n.2205+121A>G
|
|
ENST00000626839.2:c.2284A>G
|
ENSP00000486706.1:p.Asn762Asp
|
|
ENST00000629241.2:c.2133+121A>G
|
ENSP00000487142.1:n.2133+121A>G
|
|
ENST00000629676.2:c.1680-6082A>G
|
ENSP00000486194.1:n.1680-6082A>G
|
|
NM_004518.4:c.2254A>G
|
NP_004509.2:p.Asn752Asp
|
|
NM_172106.1:c.2284A>G
|
NP_742104.1:p.Asn762Asp
|
|
NM_172107.2:c.2338A>G
|
NP_742105.1:p.Asn780Asp
|
|
NM_172108.3:c.2245A>G
|
NP_742106.1:p.Asn749Asp
|
|
XM_006723787.1:c.2380A>G
|
XP_006723850.1:p.Asn794Asp
|
|
XM_011528807.1:c.2446A>G
|
XP_011527109.1:p.Asn816Asp
|
|
XM_011528808.1:c.2443A>G
|
XP_011527110.1:p.Asn815Asp
|
|
XM_011528809.1:c.2416A>G
|
XP_011527111.1:p.Asn806Asp
|
|
XM_011528810.1:c.2392A>G
|
XP_011527112.1:p.Asn798Asp
|
|
XM_011528811.1:c.2362A>G
|
XP_011527113.1:p.Asn788Asp
|
|
XM_011528812.1:c.2335A>G
|
XP_011527114.1:p.Asn779Asp
|
|
XM_011528813.1:c.2320A>G
|
XP_011527115.1:p.Asn774Asp
|
|
XM_011528814.1:c.1927A>G
|
XP_011527116.1:p.Asn643Asp
|
|
NM_004518.5:c.2254A>G
|
NP_004509.2:p.Asn752Asp
|
|
NM_172106.2:c.2284A>G
|
NP_742104.1:p.Asn762Asp
|
|
NM_172107.3:c.2338A>G
|
NP_742105.1:p.Asn780Asp
|
|
NM_172108.4:c.2245A>G
|
NP_742106.1:p.Asn749Asp
|
|
XM_011528810.2:c.2392A>G
|
XP_011527112.1:p.Asn798Asp
|
|
XM_011528811.2:c.2362A>G
|
XP_011527113.1:p.Asn788Asp
|
|
XM_017027841.2:c.2389A>G
|
XP_016883330.1:p.Asn797Asp
|
|
XM_017027842.2:c.2326A>G
|
XP_016883331.1:p.Asn776Asp
|
|
XM_017027843.1:c.2323A>G
|
XP_016883332.1:p.Asn775Asp
|
|
XM_017027844.2:c.2281A>G
|
XP_016883333.1:p.Asn761Asp
|
|
XM_017027845.1:c.1354A>G
|
XP_016883334.1:p.Asn452Asp
|
|
NM_004518.6:c.2254A>G
|
NP_004509.2:p.Asn752Asp
|
|
NM_172106.3:c.2284A>G
|
NP_742104.1:p.Asn762Asp
|
|
NM_172107.4:c.2338A>G
MANE Select
|
NP_742105.1:p.Asn780Asp
|
|
NM_172108.5:c.2245A>G
|
NP_742106.1:p.Asn749Asp
|
|
NM_001382235.1:c.2392A>G
|
NP_001369164.1:p.Asn798Asp
|
|