ENST00000399820.8:c.2577G>T
MANE Select
|
ENSP00000382717.3:p.Ala859=
|
|
ENST00000399820.7:c.2577G>T
|
ENSP00000382717.3:p.Ala859=
|
|
ENST00000506869.5:c.*2158G>T
|
ENSP00000424319.1:n.*2158G>T
|
|
ENST00000512095.5:n.1575G>T
|
|
|
NM_025132.3:c.2577G>T
|
NP_079408.3:p.Ala859=
|
|
XM_011513724.1:c.2589G>T
|
XP_011512026.1:p.Ala863=
|
|
XM_011513725.1:c.2523G>T
|
XP_011512027.1:p.Ala841=
|
|
XM_011513726.1:c.2109G>T
|
XP_011512028.1:p.Ala703=
|
|
XM_011513727.1:c.2109G>T
|
XP_011512029.1:p.Ala703=
|
|
XM_011513728.1:c.2097G>T
|
XP_011512030.1:p.Ala699=
|
|
XM_011513729.1:c.2589G>T
|
XP_011512031.1:p.Ala863=
|
|
XR_925155.1:n.2653G>T
|
|
|
NM_001317924.1:c.2097G>T
|
NP_001304853.1:p.Ala699=
|
|
XM_011513725.2:c.2523G>T
|
XP_011512027.1:p.Ala841=
|
|
XM_011513726.3:c.2109G>T
|
XP_011512028.1:p.Ala703=
|
|
XM_017008501.1:c.2097G>T
|
XP_016863990.1:p.Ala699=
|
|
XR_001741306.1:n.2653G>T
|
|
|
XR_001741307.1:n.2641G>T
|
|
|
XR_001741308.1:n.2653G>T
|
|
|
XR_001741309.1:n.2641G>T
|
|
|
XR_001741310.1:n.2641G>T
|
|
|
XR_001741311.2:n.2490G>T
|
|
|
NM_025132.4:c.2577G>T
MANE Select
|
NP_079408.3:p.Ala859=
|
|
NM_001317924.2:c.2097G>T
|
NP_001304853.1:p.Ala699=
|
|