|
ENST00000397594.7:c.*20-19G>A
(HRAS)
|
ENSP00000380722.3:n.*20-19G>A
|
|
|
ENST00000417302.7:c.*126G>A
(HRAS)
MANE Plus Clinical
|
ENSP00000388246.1:n.*126G>A
|
|
|
ENST00000397594.6:c.251-19G>A
(HRAS)
|
ENSP00000380722.2:n.251-19G>A
|
|
|
ENST00000417302.6:c.*126G>A
(HRAS)
|
ENSP00000388246.1:n.*126G>A
|
|
|
ENST00000462734.2:c.*169G>A
(HRAS)
|
ENSP00000507303.1:n.*169G>A
|
|
|
ENST00000311189.8:c.557G>A
(HRAS)
MANE Select
|
ENSP00000309845.7:p.Cys186Tyr
|
|
|
ENST00000311189.7:c.557G>A
(HRAS)
|
ENSP00000309845.7:p.Cys186Tyr
|
|
|
ENST00000397594.5:c.*126G>A
(HRAS)
|
ENSP00000380722.1:n.*126G>A
|
|
|
ENST00000397596.6:c.557G>A
(HRAS)
|
ENSP00000380723.2:p.Cys186Tyr
|
|
|
ENST00000417302.5:c.*126G>A
(HRAS)
|
ENSP00000388246.1:n.*126G>A
|
|
|
ENST00000451590.5:c.557G>A
(HRAS)
|
ENSP00000407586.1:p.Cys186Tyr
|
|
|
ENST00000462734.1:n.332G>A
(HRAS)
|
|
|
|
ENST00000478324.5:n.243-19G>A
(HRAS)
|
|
|
|
ENST00000479482.1:n.478G>A
(HRAS)
|
|
|
|
ENST00000493230.5:c.*126G>A
(HRAS)
|
ENSP00000434023.1:n.*126G>A
|
|
|
NM_001130442.1:c.557G>A
(HRAS)
|
NP_001123914.1:p.Cys186Tyr
|
|
|
NM_005343.2:c.557G>A
(HRAS)
|
NP_005334.1:p.Cys186Tyr
|
|
|
NM_176795.3:c.*126G>A
(HRAS)
|
NP_789765.1:n.*126G>A
|
|
|
XM_011519875.1:c.-425+4312C>T
(LRRC56)
|
XP_011518177.1:n.-425+4312C>T
|
|
|
XM_011519877.1:c.-162+4312C>T
(LRRC56)
|
XP_011518179.1:n.-162+4312C>T
|
|
|
XR_242795.1:n.838G>A
(HRAS)
|
|
|
|
NM_001130442.2:c.557G>A
(HRAS)
|
NP_001123914.1:p.Cys186Tyr
|
|
|
NM_001318054.1:c.320G>A
(HRAS)
|
NP_001304983.1:p.Cys107Tyr
|
|
|
NM_005343.3:c.557G>A
(HRAS)
|
NP_005334.1:p.Cys186Tyr
|
|
|
NM_176795.4:c.*126G>A
(HRAS)
|
NP_789765.1:n.*126G>A
|
|
|
XM_011519875.2:c.-425+4312C>T
(LRRC56)
|
XP_011518177.1:n.-425+4312C>T
|
|
|
XM_011519877.2:c.-162+4312C>T
(LRRC56)
|
XP_011518179.1:n.-162+4312C>T
|
|
|
XM_017017167.1:c.-500+4312C>T
(LRRC56)
|
XP_016872656.1:n.-500+4312C>T
|
|
|
XM_017017168.1:c.-500+4312C>T
(LRRC56)
|
XP_016872657.1:n.-500+4312C>T
|
|
|
NM_005343.4:c.557G>A
(HRAS)
MANE Select
|
NP_005334.1:p.Cys186Tyr
|
|
|
NM_001318054.2:c.320G>A
(HRAS)
|
NP_001304983.1:p.Cys107Tyr
|
|
|
NM_001130442.3:c.557G>A
(HRAS)
|
NP_001123914.1:p.Cys186Tyr
|
|
|
NM_176795.5:c.*126G>A
(HRAS)
MANE Plus Clinical
|
NP_789765.1:n.*126G>A
|
|
