ENST00000399820.8:c.679T>G
MANE Select
|
ENSP00000382717.3:p.Phe227Val
|
|
ENST00000399820.7:c.679T>G
|
ENSP00000382717.3:p.Phe227Val
|
|
ENST00000503697.5:c.*147T>G
|
ENSP00000423706.1:n.*147T>G
|
|
ENST00000505055.5:c.*260T>G
|
ENSP00000425949.1:n.*260T>G
|
|
ENST00000506503.1:c.679T>G
|
ENSP00000423491.1:p.Phe227Val
|
|
ENST00000506869.5:c.*260T>G
|
ENSP00000424319.1:n.*260T>G
|
|
ENST00000511729.5:n.40+22666T>G
|
|
|
ENST00000512448.1:n.273T>G
|
|
|
NM_025132.3:c.679T>G
|
NP_079408.3:p.Phe227Val
|
|
XM_011513724.1:c.679T>G
|
XP_011512026.1:p.Phe227Val
|
|
XM_011513725.1:c.613T>G
|
XP_011512027.1:p.Phe205Val
|
|
XM_011513726.1:c.199T>G
|
XP_011512028.1:p.Phe67Val
|
|
XM_011513727.1:c.199T>G
|
XP_011512029.1:p.Phe67Val
|
|
XM_011513728.1:c.199T>G
|
XP_011512030.1:p.Phe67Val
|
|
XM_011513729.1:c.679T>G
|
XP_011512031.1:p.Phe227Val
|
|
XR_925155.1:n.743T>G
|
|
|
NM_001317924.1:c.199T>G
|
NP_001304853.1:p.Phe67Val
|
|
XM_011513725.2:c.613T>G
|
XP_011512027.1:p.Phe205Val
|
|
XM_011513726.3:c.199T>G
|
XP_011512028.1:p.Phe67Val
|
|
XM_017008501.1:c.199T>G
|
XP_016863990.1:p.Phe67Val
|
|
XR_001741306.1:n.743T>G
|
|
|
XR_001741307.1:n.743T>G
|
|
|
XR_001741308.1:n.743T>G
|
|
|
XR_001741309.1:n.743T>G
|
|
|
XR_001741310.1:n.743T>G
|
|
|
XR_001741311.2:n.592T>G
|
|
|
XR_001741312.1:n.743T>G
|
|
|
NM_025132.4:c.679T>G
MANE Select
|
NP_079408.3:p.Phe227Val
|
|
NM_001317924.2:c.199T>G
|
NP_001304853.1:p.Phe67Val
|
|