ENST00000397594.7:c.*211G>C
(HRAS)
|
ENSP00000380722.3:n.*211G>C
|
|
ENST00000417302.7:c.*336G>C
(HRAS)
MANE Plus Clinical
|
ENSP00000388246.1:n.*336G>C
|
|
ENST00000397594.6:c.442G>C
(HRAS)
|
ENSP00000380722.2:n.442G>C
|
|
ENST00000417302.6:c.*336G>C
(HRAS)
|
ENSP00000388246.1:n.*336G>C
|
|
ENST00000462734.2:c.*271G>C
(HRAS)
|
ENSP00000507303.1:n.*271G>C
|
|
ENST00000311189.8:c.*89G>C
(HRAS)
MANE Select
|
ENSP00000309845.7:n.*89G>C
|
|
ENST00000311189.7:c.*89G>C
(HRAS)
|
ENSP00000309845.7:n.*89G>C
|
|
ENST00000397594.5:c.*336G>C
(HRAS)
|
ENSP00000380722.1:n.*336G>C
|
|
ENST00000397596.6:c.*197G>C
(HRAS)
|
ENSP00000380723.2:n.*197G>C
|
|
ENST00000417302.5:c.*336G>C
(HRAS)
|
ENSP00000388246.1:n.*336G>C
|
|
ENST00000451590.5:c.*197G>C
(HRAS)
|
ENSP00000407586.1:n.*197G>C
|
|
ENST00000462734.1:n.434G>C
(HRAS)
|
|
|
ENST00000478324.5:n.434G>C
(HRAS)
|
|
|
ENST00000493230.5:c.*228G>C
(HRAS)
|
ENSP00000434023.1:n.*228G>C
|
|
NM_001130442.1:c.*197G>C
(HRAS)
|
NP_001123914.1:n.*197G>C
|
|
NM_005343.2:c.*89G>C
(HRAS)
|
NP_005334.1:n.*89G>C
|
|
NM_176795.3:c.*336G>C
(HRAS)
|
NP_789765.1:n.*336G>C
|
|
XM_011519875.1:c.-425+4102C>G
(LRRC56)
|
XP_011518177.1:n.-425+4102C>G
|
|
XM_011519877.1:c.-162+4102C>G
(LRRC56)
|
XP_011518179.1:n.-162+4102C>G
|
|
XR_242795.1:n.940G>C
(HRAS)
|
|
|
NM_001130442.2:c.*197G>C
(HRAS)
|
NP_001123914.1:n.*197G>C
|
|
NM_001318054.1:c.*89G>C
(HRAS)
|
NP_001304983.1:n.*89G>C
|
|
NM_005343.3:c.*89G>C
(HRAS)
|
NP_005334.1:n.*89G>C
|
|
NM_176795.4:c.*336G>C
(HRAS)
|
NP_789765.1:n.*336G>C
|
|
XM_011519875.2:c.-425+4102C>G
(LRRC56)
|
XP_011518177.1:n.-425+4102C>G
|
|
XM_011519877.2:c.-162+4102C>G
(LRRC56)
|
XP_011518179.1:n.-162+4102C>G
|
|
XM_017017167.1:c.-500+4102C>G
(LRRC56)
|
XP_016872656.1:n.-500+4102C>G
|
|
XM_017017168.1:c.-500+4102C>G
(LRRC56)
|
XP_016872657.1:n.-500+4102C>G
|
|
NM_005343.4:c.*89G>C
(HRAS)
MANE Select
|
NP_005334.1:n.*89G>C
|
|
NM_001318054.2:c.*89G>C
(HRAS)
|
NP_001304983.1:n.*89G>C
|
|
NM_001130442.3:c.*197G>C
(HRAS)
|
NP_001123914.1:n.*197G>C
|
|
NM_176795.5:c.*336G>C
(HRAS)
MANE Plus Clinical
|
NP_789765.1:n.*336G>C
|
|