|
ENST00000397594.7:c.*133G>T
(HRAS)
|
ENSP00000380722.3:n.*133G>T
|
|
|
ENST00000417302.7:c.*258G>T
(HRAS)
MANE Plus Clinical
|
ENSP00000388246.1:n.*258G>T
|
|
|
ENST00000397594.6:c.364G>T
(HRAS)
|
ENSP00000380722.2:n.364G>T
|
|
|
ENST00000417302.6:c.*258G>T
(HRAS)
|
ENSP00000388246.1:n.*258G>T
|
|
|
ENST00000462734.2:c.*193G>T
(HRAS)
|
ENSP00000507303.1:n.*193G>T
|
|
|
ENST00000311189.8:c.*11G>T
(HRAS)
MANE Select
|
ENSP00000309845.7:n.*11G>T
|
|
|
ENST00000311189.7:c.*11G>T
(HRAS)
|
ENSP00000309845.7:n.*11G>T
|
|
|
ENST00000397594.5:c.*258G>T
(HRAS)
|
ENSP00000380722.1:n.*258G>T
|
|
|
ENST00000397596.6:c.*119G>T
(HRAS)
|
ENSP00000380723.2:n.*119G>T
|
|
|
ENST00000417302.5:c.*258G>T
(HRAS)
|
ENSP00000388246.1:n.*258G>T
|
|
|
ENST00000451590.5:c.*119G>T
(HRAS)
|
ENSP00000407586.1:n.*119G>T
|
|
|
ENST00000462734.1:n.356G>T
(HRAS)
|
|
|
|
ENST00000478324.5:n.356G>T
(HRAS)
|
|
|
|
ENST00000493230.5:c.*150G>T
(HRAS)
|
ENSP00000434023.1:n.*150G>T
|
|
|
NM_001130442.1:c.*119G>T
(HRAS)
|
NP_001123914.1:n.*119G>T
|
|
|
NM_005343.2:c.*11G>T
(HRAS)
|
NP_005334.1:n.*11G>T
|
|
|
NM_176795.3:c.*258G>T
(HRAS)
|
NP_789765.1:n.*258G>T
|
|
|
XM_011519875.1:c.-425+4180C>A
(LRRC56)
|
XP_011518177.1:n.-425+4180C>A
|
|
|
XM_011519877.1:c.-162+4180C>A
(LRRC56)
|
XP_011518179.1:n.-162+4180C>A
|
|
|
XR_242795.1:n.862G>T
(HRAS)
|
|
|
|
NM_001130442.2:c.*119G>T
(HRAS)
|
NP_001123914.1:n.*119G>T
|
|
|
NM_001318054.1:c.*11G>T
(HRAS)
|
NP_001304983.1:n.*11G>T
|
|
|
NM_005343.3:c.*11G>T
(HRAS)
|
NP_005334.1:n.*11G>T
|
|
|
NM_176795.4:c.*258G>T
(HRAS)
|
NP_789765.1:n.*258G>T
|
|
|
XM_011519875.2:c.-425+4180C>A
(LRRC56)
|
XP_011518177.1:n.-425+4180C>A
|
|
|
XM_011519877.2:c.-162+4180C>A
(LRRC56)
|
XP_011518179.1:n.-162+4180C>A
|
|
|
XM_017017167.1:c.-500+4180C>A
(LRRC56)
|
XP_016872656.1:n.-500+4180C>A
|
|
|
XM_017017168.1:c.-500+4180C>A
(LRRC56)
|
XP_016872657.1:n.-500+4180C>A
|
|
|
NM_005343.4:c.*11G>T
(HRAS)
MANE Select
|
NP_005334.1:n.*11G>T
|
|
|
NM_001318054.2:c.*11G>T
(HRAS)
|
NP_001304983.1:n.*11G>T
|
|
|
NM_001130442.3:c.*119G>T
(HRAS)
|
NP_001123914.1:n.*119G>T
|
|
|
NM_176795.5:c.*258G>T
(HRAS)
MANE Plus Clinical
|
NP_789765.1:n.*258G>T
|
|
