ENST00000399820.8:c.2558T>C
MANE Select
|
ENSP00000382717.3:p.Met853Thr
|
|
ENST00000399820.7:c.2558T>C
|
ENSP00000382717.3:p.Met853Thr
|
|
ENST00000506869.5:c.*2139T>C
|
ENSP00000424319.1:n.*2139T>C
|
|
ENST00000512095.5:n.1556T>C
|
|
|
NM_025132.3:c.2558T>C
|
NP_079408.3:p.Met853Thr
|
|
XM_011513724.1:c.2570T>C
|
XP_011512026.1:p.Met857Thr
|
|
XM_011513725.1:c.2504T>C
|
XP_011512027.1:p.Met835Thr
|
|
XM_011513726.1:c.2090T>C
|
XP_011512028.1:p.Met697Thr
|
|
XM_011513727.1:c.2090T>C
|
XP_011512029.1:p.Met697Thr
|
|
XM_011513728.1:c.2078T>C
|
XP_011512030.1:p.Met693Thr
|
|
XM_011513729.1:c.2570T>C
|
XP_011512031.1:p.Met857Thr
|
|
XR_925155.1:n.2634T>C
|
|
|
NM_001317924.1:c.2078T>C
|
NP_001304853.1:p.Met693Thr
|
|
XM_011513725.2:c.2504T>C
|
XP_011512027.1:p.Met835Thr
|
|
XM_011513726.3:c.2090T>C
|
XP_011512028.1:p.Met697Thr
|
|
XM_017008501.1:c.2078T>C
|
XP_016863990.1:p.Met693Thr
|
|
XR_001741306.1:n.2634T>C
|
|
|
XR_001741307.1:n.2622T>C
|
|
|
XR_001741308.1:n.2634T>C
|
|
|
XR_001741309.1:n.2622T>C
|
|
|
XR_001741310.1:n.2622T>C
|
|
|
XR_001741311.2:n.2471T>C
|
|
|
NM_025132.4:c.2558T>C
MANE Select
|
NP_079408.3:p.Met853Thr
|
|
NM_001317924.2:c.2078T>C
|
NP_001304853.1:p.Met693Thr
|
|