ENST00000706989.1:c.2399G>A
|
ENSP00000516702.1:p.Arg800Gln
|
|
ENST00000359125.7:c.2345G>A
MANE Select
|
ENSP00000352035.2:p.Arg782Gln
|
|
ENST00000637193.1:c.1742G>A
|
ENSP00000490734.1:p.Arg581Gln
|
|
ENST00000344462.8:c.2252G>A
|
ENSP00000339611.4:p.Arg751Gln
|
|
ENST00000357249.6:c.1913G>A
|
ENSP00000349789.3:p.Arg638Gln
|
|
ENST00000359125.6:c.2345G>A
|
ENSP00000352035.2:p.Arg782Gln
|
|
ENST00000360480.7:c.2261G>A
|
ENSP00000353668.3:p.Arg754Gln
|
|
ENST00000370224.5:c.2241+128G>A
|
ENSP00000359244.2:n.2241+128G>A
|
|
ENST00000625514.2:c.2205+128G>A
|
ENSP00000486040.1:n.2205+128G>A
|
|
ENST00000626839.2:c.2291G>A
|
ENSP00000486706.1:p.Arg764Gln
|
|
ENST00000629241.2:c.2133+128G>A
|
ENSP00000487142.1:n.2133+128G>A
|
|
ENST00000629676.2:c.1680-6075G>A
|
ENSP00000486194.1:n.1680-6075G>A
|
|
NM_004518.4:c.2261G>A
|
NP_004509.2:p.Arg754Gln
|
|
NM_172106.1:c.2291G>A
|
NP_742104.1:p.Arg764Gln
|
|
NM_172107.2:c.2345G>A
|
NP_742105.1:p.Arg782Gln
|
|
NM_172108.3:c.2252G>A
|
NP_742106.1:p.Arg751Gln
|
|
XM_006723787.1:c.2387G>A
|
XP_006723850.1:p.Arg796Gln
|
|
XM_011528807.1:c.2453G>A
|
XP_011527109.1:p.Arg818Gln
|
|
XM_011528808.1:c.2450G>A
|
XP_011527110.1:p.Arg817Gln
|
|
XM_011528809.1:c.2423G>A
|
XP_011527111.1:p.Arg808Gln
|
|
XM_011528810.1:c.2399G>A
|
XP_011527112.1:p.Arg800Gln
|
|
XM_011528811.1:c.2369G>A
|
XP_011527113.1:p.Arg790Gln
|
|
XM_011528812.1:c.2342G>A
|
XP_011527114.1:p.Arg781Gln
|
|
XM_011528813.1:c.2327G>A
|
XP_011527115.1:p.Arg776Gln
|
|
XM_011528814.1:c.1934G>A
|
XP_011527116.1:p.Arg645Gln
|
|
NM_004518.5:c.2261G>A
|
NP_004509.2:p.Arg754Gln
|
|
NM_172106.2:c.2291G>A
|
NP_742104.1:p.Arg764Gln
|
|
NM_172107.3:c.2345G>A
|
NP_742105.1:p.Arg782Gln
|
|
NM_172108.4:c.2252G>A
|
NP_742106.1:p.Arg751Gln
|
|
XM_011528810.2:c.2399G>A
|
XP_011527112.1:p.Arg800Gln
|
|
XM_011528811.2:c.2369G>A
|
XP_011527113.1:p.Arg790Gln
|
|
XM_017027841.2:c.2396G>A
|
XP_016883330.1:p.Arg799Gln
|
|
XM_017027842.2:c.2333G>A
|
XP_016883331.1:p.Arg778Gln
|
|
XM_017027843.1:c.2330G>A
|
XP_016883332.1:p.Arg777Gln
|
|
XM_017027844.2:c.2288G>A
|
XP_016883333.1:p.Arg763Gln
|
|
XM_017027845.1:c.1361G>A
|
XP_016883334.1:p.Arg454Gln
|
|
NM_004518.6:c.2261G>A
|
NP_004509.2:p.Arg754Gln
|
|
NM_172106.3:c.2291G>A
|
NP_742104.1:p.Arg764Gln
|
|
NM_172107.4:c.2345G>A
MANE Select
|
NP_742105.1:p.Arg782Gln
|
|
NM_172108.5:c.2252G>A
|
NP_742106.1:p.Arg751Gln
|
|
NM_001382235.1:c.2399G>A
|
NP_001369164.1:p.Arg800Gln
|
|