|
ENST00000685328.1:c.*1599T>G
(KRAS)
|
ENSP00000508921.1:n.*1599T>G
|
|
|
ENST00000686877.1:c.*2137T>G
(KRAS)
|
ENSP00000510431.1:n.*2137T>G
|
|
|
ENST00000687356.1:c.*1864T>G
(KRAS)
|
ENSP00000510511.1:n.*1864T>G
|
|
|
ENST00000688940.1:c.*1599T>G
(KRAS)
|
ENSP00000509238.1:n.*1599T>G
|
|
|
ENST00000690406.1:c.1969T>G
(KRAS)
|
|
|
|
ENST00000690804.1:c.*2127T>G
(KRAS)
|
ENSP00000508568.1:n.*2127T>G
|
|
|
ENST00000692768.1:c.*1599T>G
(KRAS)
|
ENSP00000510254.1:n.*1599T>G
|
|
|
ENST00000693229.1:c.*1599T>G
(KRAS)
|
ENSP00000509223.1:n.*1599T>G
|
|
|
ENST00000256078.10:c.*1720T>G
(KRAS)
MANE Plus Clinical
|
ENSP00000256078.5:n.*1720T>G
|
|
|
ENST00000311936.8:c.*1599T>G
(KRAS)
MANE Select
|
ENSP00000308495.3:n.*1599T>G
|
|
|
ENST00000553788.6:c.52-999A>C
(ETFRF1)
|
ENSP00000451938.2:n.52-999A>C
|
|
|
ENST00000311936.7:c.*1599T>G
(KRAS)
|
ENSP00000308495.3:n.*1599T>G
|
|
|
ENST00000553788.5:c.46-999A>C
(ETFRF1)
|
ENSP00000451938.1:n.46-999A>C
|
|
|
NM_004985.4:c.*1599T>G
(KRAS)
|
NP_004976.2:n.*1599T>G
|
|
|
NM_033360.3:c.*1720T>G
(KRAS)
|
NP_203524.1:n.*1720T>G
|
|
|
XM_011520653.1:c.*1599T>G
(KRAS)
|
XP_011518955.1:n.*1599T>G
|
|
|
XM_011520653.3:c.*1599T>G
(KRAS)
|
XP_011518955.1:n.*1599T>G
|
|
|
NM_001369786.1:c.*1720T>G
(KRAS)
|
NP_001356715.1:n.*1720T>G
|
|
|
NM_001369787.1:c.*1599T>G
(KRAS)
|
NP_001356716.1:n.*1599T>G
|
|
|
NM_004985.5:c.*1599T>G
(KRAS)
MANE Select
|
NP_004976.2:n.*1599T>G
|
|
|
NM_033360.4:c.*1720T>G
(KRAS)
MANE Plus Clinical
|
NP_203524.1:n.*1720T>G
|
|
