ENST00000706989.1:c.2653T>A
|
ENSP00000516702.1:p.Trp885Arg
|
|
ENST00000359125.7:c.2599T>A
MANE Select
|
ENSP00000352035.2:p.Trp867Arg
|
|
ENST00000637193.1:c.1996T>A
|
ENSP00000490734.1:p.Trp666Arg
|
|
ENST00000344462.8:c.2506T>A
|
ENSP00000339611.4:p.Trp836Arg
|
|
ENST00000357249.6:c.2167T>A
|
ENSP00000349789.3:p.Trp723Arg
|
|
ENST00000359125.6:c.2599T>A
|
ENSP00000352035.2:p.Trp867Arg
|
|
ENST00000360480.7:c.2515T>A
|
ENSP00000353668.3:p.Trp839Arg
|
|
ENST00000370224.5:c.2241+382T>A
|
ENSP00000359244.2:n.2241+382T>A
|
|
ENST00000625514.2:c.2205+382T>A
|
ENSP00000486040.1:n.2205+382T>A
|
|
ENST00000626839.2:c.2545T>A
|
ENSP00000486706.1:p.Trp849Arg
|
|
ENST00000629241.2:c.2133+382T>A
|
ENSP00000487142.1:n.2133+382T>A
|
|
ENST00000629676.2:c.1680-5821T>A
|
ENSP00000486194.1:n.1680-5821T>A
|
|
NM_004518.4:c.2515T>A
|
NP_004509.2:p.Trp839Arg
|
|
NM_172106.1:c.2545T>A
|
NP_742104.1:p.Trp849Arg
|
|
NM_172107.2:c.2599T>A
|
NP_742105.1:p.Trp867Arg
|
|
NM_172108.3:c.2506T>A
|
NP_742106.1:p.Trp836Arg
|
|
XM_006723787.1:c.2641T>A
|
XP_006723850.1:p.Trp881Arg
|
|
XM_011528807.1:c.2707T>A
|
XP_011527109.1:p.Trp903Arg
|
|
XM_011528808.1:c.2704T>A
|
XP_011527110.1:p.Trp902Arg
|
|
XM_011528809.1:c.2677T>A
|
XP_011527111.1:p.Trp893Arg
|
|
XM_011528810.1:c.2653T>A
|
XP_011527112.1:p.Trp885Arg
|
|
XM_011528811.1:c.2623T>A
|
XP_011527113.1:p.Trp875Arg
|
|
XM_011528812.1:c.2596T>A
|
XP_011527114.1:p.Trp866Arg
|
|
XM_011528813.1:c.2581T>A
|
XP_011527115.1:p.Trp861Arg
|
|
XM_011528814.1:c.2188T>A
|
XP_011527116.1:p.Trp730Arg
|
|
NM_004518.5:c.2515T>A
|
NP_004509.2:p.Trp839Arg
|
|
NM_172106.2:c.2545T>A
|
NP_742104.1:p.Trp849Arg
|
|
NM_172107.3:c.2599T>A
|
NP_742105.1:p.Trp867Arg
|
|
NM_172108.4:c.2506T>A
|
NP_742106.1:p.Trp836Arg
|
|
XM_011528810.2:c.2653T>A
|
XP_011527112.1:p.Trp885Arg
|
|
XM_011528811.2:c.2623T>A
|
XP_011527113.1:p.Trp875Arg
|
|
XM_017027841.2:c.2650T>A
|
XP_016883330.1:p.Trp884Arg
|
|
XM_017027842.2:c.2587T>A
|
XP_016883331.1:p.Trp863Arg
|
|
XM_017027843.1:c.2584T>A
|
XP_016883332.1:p.Trp862Arg
|
|
XM_017027844.2:c.2542T>A
|
XP_016883333.1:p.Trp848Arg
|
|
XM_017027845.1:c.1615T>A
|
XP_016883334.1:p.Trp539Arg
|
|
NM_004518.6:c.2515T>A
|
NP_004509.2:p.Trp839Arg
|
|
NM_172106.3:c.2545T>A
|
NP_742104.1:p.Trp849Arg
|
|
NM_172107.4:c.2599T>A
MANE Select
|
NP_742105.1:p.Trp867Arg
|
|
NM_172108.5:c.2506T>A
|
NP_742106.1:p.Trp836Arg
|
|
NM_001382235.1:c.2653T>A
|
NP_001369164.1:p.Trp885Arg
|
|