ENST00000399820.8:c.3724G=
MANE Select
|
ENSP00000382717.3:p.Asp1242=
|
|
ENST00000399820.7:c.3724G=
|
ENSP00000382717.3:p.Asp1242=
|
|
ENST00000503733.1:n.64G=
|
|
|
ENST00000506869.5:c.*3305G=
|
ENSP00000424319.1:n.*3305G=
|
|
ENST00000512534.5:n.2035G=
|
|
|
ENST00000512588.5:n.66G=
|
|
|
NM_025132.3:c.3724G=
|
NP_079408.3:p.Asp1242=
|
|
XM_011513724.1:c.3736G=
|
XP_011512026.1:p.Asp1246=
|
|
XM_011513725.1:c.3670G=
|
XP_011512027.1:p.Asp1224=
|
|
XM_011513726.1:c.3256G=
|
XP_011512028.1:p.Asp1086=
|
|
XM_011513727.1:c.3256G=
|
XP_011512029.1:p.Asp1086=
|
|
XM_011513728.1:c.3244G=
|
XP_011512030.1:p.Asp1082=
|
|
XR_925155.1:n.5434G=
|
|
|
NM_001317924.1:c.3244G=
|
NP_001304853.1:p.Asp1082=
|
|
XM_011513725.2:c.3670G=
|
XP_011512027.1:p.Asp1224=
|
|
XM_011513726.3:c.3256G=
|
XP_011512028.1:p.Asp1086=
|
|
XM_017008501.1:c.3244G=
|
XP_016863990.1:p.Asp1082=
|
|
XR_001741306.1:n.4001G=
|
|
|
XR_001741307.1:n.3989G=
|
|
|
XR_001741308.1:n.5635G=
|
|
|
XR_001741309.1:n.5422G=
|
|
|
XR_001741310.1:n.5623G=
|
|
|
XR_001741311.2:n.5271G=
|
|
|
NM_025132.4:c.3724G=
MANE Select
|
NP_079408.3:p.Asp1242=
|
|
NM_001317924.2:c.3244G=
|
NP_001304853.1:p.Asp1082=
|
|