ENST00000399820.8:c.3717G>A
MANE Select
|
ENSP00000382717.3:p.Arg1239=
|
|
ENST00000399820.7:c.3717G>A
|
ENSP00000382717.3:p.Arg1239=
|
|
ENST00000503733.1:n.57G>A
|
|
|
ENST00000506869.5:c.*3298G>A
|
ENSP00000424319.1:n.*3298G>A
|
|
ENST00000512534.5:n.2028G>A
|
|
|
ENST00000512588.5:n.59G>A
|
|
|
NM_025132.3:c.3717G>A
|
NP_079408.3:p.Arg1239=
|
|
XM_011513724.1:c.3729G>A
|
XP_011512026.1:p.Arg1243=
|
|
XM_011513725.1:c.3663G>A
|
XP_011512027.1:p.Arg1221=
|
|
XM_011513726.1:c.3249G>A
|
XP_011512028.1:p.Arg1083=
|
|
XM_011513727.1:c.3249G>A
|
XP_011512029.1:p.Arg1083=
|
|
XM_011513728.1:c.3237G>A
|
XP_011512030.1:p.Arg1079=
|
|
XR_925155.1:n.5427G>A
|
|
|
NM_001317924.1:c.3237G>A
|
NP_001304853.1:p.Arg1079=
|
|
XM_011513725.2:c.3663G>A
|
XP_011512027.1:p.Arg1221=
|
|
XM_011513726.3:c.3249G>A
|
XP_011512028.1:p.Arg1083=
|
|
XM_017008501.1:c.3237G>A
|
XP_016863990.1:p.Arg1079=
|
|
XR_001741306.1:n.3994G>A
|
|
|
XR_001741307.1:n.3982G>A
|
|
|
XR_001741308.1:n.5628G>A
|
|
|
XR_001741309.1:n.5415G>A
|
|
|
XR_001741310.1:n.5616G>A
|
|
|
XR_001741311.2:n.5264G>A
|
|
|
NM_025132.4:c.3717G>A
MANE Select
|
NP_079408.3:p.Arg1239=
|
|
NM_001317924.2:c.3237G>A
|
NP_001304853.1:p.Arg1079=
|
|