ENST00000399820.8:c.3800G=
MANE Select
|
ENSP00000382717.3:p.Cys1267=
|
|
ENST00000399820.7:c.3800G=
|
ENSP00000382717.3:p.Cys1267=
|
|
ENST00000503733.1:n.140G=
|
|
|
ENST00000506869.5:c.*3381G=
|
ENSP00000424319.1:n.*3381G=
|
|
ENST00000512534.5:n.2111G=
|
|
|
ENST00000512588.5:n.142G=
|
|
|
NM_025132.3:c.3800G=
|
NP_079408.3:p.Cys1267=
|
|
XM_011513724.1:c.3812G=
|
XP_011512026.1:p.Cys1271=
|
|
XM_011513725.1:c.3746G=
|
XP_011512027.1:p.Cys1249=
|
|
XM_011513726.1:c.3332G=
|
XP_011512028.1:p.Cys1111=
|
|
XM_011513727.1:c.3332G=
|
XP_011512029.1:p.Cys1111=
|
|
XM_011513728.1:c.3320G=
|
XP_011512030.1:p.Cys1107=
|
|
XR_925155.1:n.5510G=
|
|
|
NM_001317924.1:c.3320G=
|
NP_001304853.1:p.Cys1107=
|
|
XM_011513725.2:c.3746G=
|
XP_011512027.1:p.Cys1249=
|
|
XM_011513726.3:c.3332G=
|
XP_011512028.1:p.Cys1111=
|
|
XM_017008501.1:c.3320G=
|
XP_016863990.1:p.Cys1107=
|
|
XR_001741306.1:n.4077G=
|
|
|
XR_001741307.1:n.4065G=
|
|
|
XR_001741308.1:n.5711G=
|
|
|
XR_001741309.1:n.5498G=
|
|
|
XR_001741310.1:n.5699G=
|
|
|
XR_001741311.2:n.5347G=
|
|
|
NM_025132.4:c.3800G=
MANE Select
|
NP_079408.3:p.Cys1267=
|
|
NM_001317924.2:c.3320G=
|
NP_001304853.1:p.Cys1107=
|
|