ENST00000397594.7:c.398T>A
(HRAS)
|
ENSP00000380722.3:p.Leu133His
|
|
ENST00000417302.7:c.398T>A
(HRAS)
MANE Plus Clinical
|
ENSP00000388246.1:p.Leu133His
|
|
ENST00000397594.6:c.116T>A
(HRAS)
|
ENSP00000380722.2:p.Leu39His
|
|
ENST00000417302.6:c.398T>A
(HRAS)
|
ENSP00000388246.1:p.Leu133His
|
|
ENST00000462734.2:c.398T>A
(HRAS)
|
ENSP00000507303.1:p.Leu133His
|
|
ENST00000311189.8:c.398T>A
(HRAS)
MANE Select
|
ENSP00000309845.7:p.Leu133His
|
|
ENST00000311189.7:c.398T>A
(HRAS)
|
ENSP00000309845.7:p.Leu133His
|
|
ENST00000397594.5:c.398T>A
(HRAS)
|
ENSP00000380722.1:p.Leu133His
|
|
ENST00000397596.6:c.398T>A
(HRAS)
|
ENSP00000380723.2:p.Leu133His
|
|
ENST00000417302.5:c.398T>A
(HRAS)
|
ENSP00000388246.1:p.Leu133His
|
|
ENST00000451590.5:c.398T>A
(HRAS)
|
ENSP00000407586.1:p.Leu133His
|
|
ENST00000462734.1:n.91T>A
(HRAS)
|
|
|
ENST00000478324.5:n.108T>A
(HRAS)
|
|
|
ENST00000479482.1:n.319T>A
(HRAS)
|
|
|
ENST00000493230.5:c.398T>A
(HRAS)
|
ENSP00000434023.1:p.Leu133His
|
|
NM_001130442.1:c.398T>A
(HRAS)
|
NP_001123914.1:p.Leu133His
|
|
NM_005343.2:c.398T>A
(HRAS)
|
NP_005334.1:p.Leu133His
|
|
NM_176795.3:c.398T>A
(HRAS)
|
NP_789765.1:p.Leu133His
|
|
XM_011519875.1:c.-424-5093A>T
(LRRC56)
|
XP_011518177.1:n.-424-5093A>T
|
|
XM_011519877.1:c.-162+5168A>T
(LRRC56)
|
XP_011518179.1:n.-162+5168A>T
|
|
XR_242795.1:n.597T>A
(HRAS)
|
|
|
NM_001130442.2:c.398T>A
(HRAS)
|
NP_001123914.1:p.Leu133His
|
|
NM_001318054.1:c.79T>A
(HRAS)
|
NP_001304983.1:p.Ser27Thr
|
|
NM_005343.3:c.398T>A
(HRAS)
|
NP_005334.1:p.Leu133His
|
|
NM_176795.4:c.398T>A
(HRAS)
|
NP_789765.1:p.Leu133His
|
|
XM_011519875.2:c.-424-5093A>T
(LRRC56)
|
XP_011518177.1:n.-424-5093A>T
|
|
XM_011519877.2:c.-162+5168A>T
(LRRC56)
|
XP_011518179.1:n.-162+5168A>T
|
|
XM_017017167.1:c.-499-5018A>T
(LRRC56)
|
XP_016872656.1:n.-499-5018A>T
|
|
XM_017017168.1:c.-499-5018A>T
(LRRC56)
|
XP_016872657.1:n.-499-5018A>T
|
|
NM_005343.4:c.398T>A
(HRAS)
MANE Select
|
NP_005334.1:p.Leu133His
|
|
NM_001318054.2:c.79T>A
(HRAS)
|
NP_001304983.1:p.Ser27Thr
|
|
NM_001130442.3:c.398T>A
(HRAS)
|
NP_001123914.1:p.Leu133His
|
|
NM_176795.5:c.398T>A
(HRAS)
MANE Plus Clinical
|
NP_789765.1:p.Leu133His
|
|