ENST00000399820.8:c.2533G>T
MANE Select
|
ENSP00000382717.3:p.Asp845Tyr
|
|
ENST00000399820.7:c.2533G>T
|
ENSP00000382717.3:p.Asp845Tyr
|
|
ENST00000506869.5:c.*2114G>T
|
ENSP00000424319.1:n.*2114G>T
|
|
ENST00000512095.5:n.1531G>T
|
|
|
NM_025132.3:c.2533G>T
|
NP_079408.3:p.Asp845Tyr
|
|
XM_011513724.1:c.2545G>T
|
XP_011512026.1:p.Asp849Tyr
|
|
XM_011513725.1:c.2479G>T
|
XP_011512027.1:p.Asp827Tyr
|
|
XM_011513726.1:c.2065G>T
|
XP_011512028.1:p.Asp689Tyr
|
|
XM_011513727.1:c.2065G>T
|
XP_011512029.1:p.Asp689Tyr
|
|
XM_011513728.1:c.2053G>T
|
XP_011512030.1:p.Asp685Tyr
|
|
XM_011513729.1:c.2545G>T
|
XP_011512031.1:p.Asp849Tyr
|
|
XR_925155.1:n.2609G>T
|
|
|
NM_001317924.1:c.2053G>T
|
NP_001304853.1:p.Asp685Tyr
|
|
XM_011513725.2:c.2479G>T
|
XP_011512027.1:p.Asp827Tyr
|
|
XM_011513726.3:c.2065G>T
|
XP_011512028.1:p.Asp689Tyr
|
|
XM_017008501.1:c.2053G>T
|
XP_016863990.1:p.Asp685Tyr
|
|
XR_001741306.1:n.2609G>T
|
|
|
XR_001741307.1:n.2597G>T
|
|
|
XR_001741308.1:n.2609G>T
|
|
|
XR_001741309.1:n.2597G>T
|
|
|
XR_001741310.1:n.2597G>T
|
|
|
XR_001741311.2:n.2446G>T
|
|
|
NM_025132.4:c.2533G>T
MANE Select
|
NP_079408.3:p.Asp845Tyr
|
|
NM_001317924.2:c.2053G>T
|
NP_001304853.1:p.Asp685Tyr
|
|