ENST00000399820.8:c.3810T>C
MANE Select
|
ENSP00000382717.3:p.Cys1270=
|
|
ENST00000399820.7:c.3810T>C
|
ENSP00000382717.3:p.Cys1270=
|
|
ENST00000503733.1:n.150T>C
|
|
|
ENST00000506869.5:c.*3391T>C
|
ENSP00000424319.1:n.*3391T>C
|
|
ENST00000512534.5:n.2121T>C
|
|
|
ENST00000512588.5:n.152T>C
|
|
|
NM_025132.3:c.3810T>C
|
NP_079408.3:p.Cys1270=
|
|
XM_011513724.1:c.3822T>C
|
XP_011512026.1:p.Cys1274=
|
|
XM_011513725.1:c.3756T>C
|
XP_011512027.1:p.Cys1252=
|
|
XM_011513726.1:c.3342T>C
|
XP_011512028.1:p.Cys1114=
|
|
XM_011513727.1:c.3342T>C
|
XP_011512029.1:p.Cys1114=
|
|
XM_011513728.1:c.3330T>C
|
XP_011512030.1:p.Cys1110=
|
|
XR_925155.1:n.5520T>C
|
|
|
NM_001317924.1:c.3330T>C
|
NP_001304853.1:p.Cys1110=
|
|
XM_011513725.2:c.3756T>C
|
XP_011512027.1:p.Cys1252=
|
|
XM_011513726.3:c.3342T>C
|
XP_011512028.1:p.Cys1114=
|
|
XM_017008501.1:c.3330T>C
|
XP_016863990.1:p.Cys1110=
|
|
XR_001741306.1:n.4087T>C
|
|
|
XR_001741307.1:n.4075T>C
|
|
|
XR_001741308.1:n.5721T>C
|
|
|
XR_001741309.1:n.5508T>C
|
|
|
XR_001741310.1:n.5709T>C
|
|
|
XR_001741311.2:n.5357T>C
|
|
|
NM_025132.4:c.3810T>C
MANE Select
|
NP_079408.3:p.Cys1270=
|
|
NM_001317924.2:c.3330T>C
|
NP_001304853.1:p.Cys1110=
|
|