|
ENST00000397594.7:c.4A>T
(HRAS)
|
ENSP00000380722.3:p.Thr2Ser
|
|
|
ENST00000417302.7:c.4A>T
(HRAS)
MANE Plus Clinical
|
ENSP00000388246.1:p.Thr2Ser
|
|
|
ENST00000417302.6:c.4A>T
(HRAS)
|
ENSP00000388246.1:p.Thr2Ser
|
|
|
ENST00000462734.2:c.4A>T
(HRAS)
|
ENSP00000507303.1:p.Thr2Ser
|
|
|
ENST00000311189.8:c.4A>T
(HRAS)
MANE Select
|
ENSP00000309845.7:p.Thr2Ser
|
|
|
ENST00000311189.7:c.4A>T
(HRAS)
|
ENSP00000309845.7:p.Thr2Ser
|
|
|
ENST00000397594.5:c.4A>T
(HRAS)
|
ENSP00000380722.1:p.Thr2Ser
|
|
|
ENST00000397596.6:c.4A>T
(HRAS)
|
ENSP00000380723.2:p.Thr2Ser
|
|
|
ENST00000417302.5:c.4A>T
(HRAS)
|
ENSP00000388246.1:p.Thr2Ser
|
|
|
ENST00000451590.5:c.4A>T
(HRAS)
|
ENSP00000407586.1:p.Thr2Ser
|
|
|
ENST00000468682.2:n.492A>T
(HRAS)
|
|
|
|
ENST00000482021.1:n.127A>T
(HRAS)
|
|
|
|
ENST00000493230.5:c.4A>T
(HRAS)
|
ENSP00000434023.1:p.Thr2Ser
|
|
|
NM_001130442.1:c.4A>T
(HRAS)
|
NP_001123914.1:p.Thr2Ser
|
|
|
NM_005343.2:c.4A>T
(HRAS)
|
NP_005334.1:p.Thr2Ser
|
|
|
NM_176795.3:c.4A>T
(HRAS)
|
NP_789765.1:p.Thr2Ser
|
|
|
XM_011519875.1:c.-424-4279T>A
(LRRC56)
|
XP_011518177.1:n.-424-4279T>A
|
|
|
XM_011519877.1:c.-161-5261T>A
(LRRC56)
|
XP_011518179.1:n.-161-5261T>A
|
|
|
XR_242795.1:n.203A>T
(HRAS)
|
|
|
|
NM_001130442.2:c.4A>T
(HRAS)
|
NP_001123914.1:p.Thr2Ser
|
|
|
NM_001318054.1:c.-316A>T
(HRAS)
|
NP_001304983.1:n.-316A>T
|
|
|
NM_005343.3:c.4A>T
(HRAS)
|
NP_005334.1:p.Thr2Ser
|
|
|
NM_176795.4:c.4A>T
(HRAS)
|
NP_789765.1:p.Thr2Ser
|
|
|
XM_011519875.2:c.-424-4279T>A
(LRRC56)
|
XP_011518177.1:n.-424-4279T>A
|
|
|
XM_011519877.2:c.-161-5261T>A
(LRRC56)
|
XP_011518179.1:n.-161-5261T>A
|
|
|
XM_017017167.1:c.-499-4204T>A
(LRRC56)
|
XP_016872656.1:n.-499-4204T>A
|
|
|
XM_017017168.1:c.-499-4204T>A
(LRRC56)
|
XP_016872657.1:n.-499-4204T>A
|
|
|
NM_005343.4:c.4A>T
(HRAS)
MANE Select
|
NP_005334.1:p.Thr2Ser
|
|
|
NM_001318054.2:c.-316A>T
(HRAS)
|
NP_001304983.1:n.-316A>T
|
|
|
NM_001130442.3:c.4A>T
(HRAS)
|
NP_001123914.1:p.Thr2Ser
|
|
|
NM_176795.5:c.4A>T
(HRAS)
MANE Plus Clinical
|
NP_789765.1:p.Thr2Ser
|
|
