ENST00000399820.8:c.848T>G
MANE Select
|
ENSP00000382717.3:p.Val283Gly
|
|
ENST00000399820.7:c.848T>G
|
ENSP00000382717.3:p.Val283Gly
|
|
ENST00000503697.5:c.*316T>G
|
ENSP00000423706.1:n.*316T>G
|
|
ENST00000506503.1:c.848T>G
|
ENSP00000423491.1:p.Val283Gly
|
|
ENST00000506869.5:c.*429T>G
|
ENSP00000424319.1:n.*429T>G
|
|
ENST00000511729.5:n.41-22864T>G
|
|
|
ENST00000512448.1:n.442T>G
|
|
|
NM_025132.3:c.848T>G
|
NP_079408.3:p.Val283Gly
|
|
XM_011513724.1:c.848T>G
|
XP_011512026.1:p.Val283Gly
|
|
XM_011513725.1:c.782T>G
|
XP_011512027.1:p.Val261Gly
|
|
XM_011513726.1:c.368T>G
|
XP_011512028.1:p.Val123Gly
|
|
XM_011513727.1:c.368T>G
|
XP_011512029.1:p.Val123Gly
|
|
XM_011513728.1:c.368T>G
|
XP_011512030.1:p.Val123Gly
|
|
XM_011513729.1:c.848T>G
|
XP_011512031.1:p.Val283Gly
|
|
XR_925155.1:n.912T>G
|
|
|
NM_001317924.1:c.368T>G
|
NP_001304853.1:p.Val123Gly
|
|
XM_011513725.2:c.782T>G
|
XP_011512027.1:p.Val261Gly
|
|
XM_011513726.3:c.368T>G
|
XP_011512028.1:p.Val123Gly
|
|
XM_017008501.1:c.368T>G
|
XP_016863990.1:p.Val123Gly
|
|
XR_001741306.1:n.912T>G
|
|
|
XR_001741307.1:n.912T>G
|
|
|
XR_001741308.1:n.912T>G
|
|
|
XR_001741309.1:n.912T>G
|
|
|
XR_001741310.1:n.912T>G
|
|
|
XR_001741311.2:n.761T>G
|
|
|
XR_001741312.1:n.912T>G
|
|
|
NM_025132.4:c.848T>G
MANE Select
|
NP_079408.3:p.Val283Gly
|
|
NM_001317924.2:c.368T>G
|
NP_001304853.1:p.Val123Gly
|
|