|
ENST00000450046.2:c.2148G>T
(EGFR)
|
ENSP00000413354.2:p.Val716=
|
|
|
ENST00000700145.1:c.656G>T
(EGFR)
|
|
|
|
ENST00000275493.7:c.2307G>T
(EGFR)
MANE Select
|
ENSP00000275493.2:p.Val769=
|
|
|
ENST00000275493.6:c.2307G>T
(EGFR)
|
ENSP00000275493.2:p.Val769=
|
|
|
ENST00000442591.5:c.*28+8388G>T
(EGFR)
|
ENSP00000410031.1:n.*28+8388G>T
|
|
|
ENST00000454757.6:c.2172G>T
(EGFR)
|
ENSP00000395243.3:p.Val724=
|
|
|
ENST00000455089.5:c.2172G>T
(EGFR)
|
ENSP00000415559.1:p.Val724=
|
|
|
NM_005228.3:c.2307G>T , LRG_304t1:c.2307G>T
(EGFR)
|
NP_005219.2:p.Val769=
|
|
|
NR_047551.1:n.1255C>A
(EGFR-AS1)
|
|
|
|
NM_001346897.1:c.2172G>T
(EGFR)
|
NP_001333826.1:p.Val724=
|
|
|
NM_001346898.1:c.2307G>T
(EGFR)
|
NP_001333827.1:p.Val769=
|
|
|
NM_001346899.1:c.2172G>T
(EGFR)
|
NP_001333828.1:p.Val724=
|
|
|
NM_001346900.1:c.2148G>T
(EGFR)
|
NP_001333829.1:p.Val716=
|
|
|
NM_001346941.1:c.1506G>T
(EGFR)
|
NP_001333870.1:p.Val502=
|
|
|
NM_005228.4:c.2307G>T
(EGFR)
|
NP_005219.2:p.Val769=
|
|
|
NM_005228.5:c.2307G>T
(EGFR)
MANE Select
|
NP_005219.2:p.Val769=
|
|
|
NM_001346897.2:c.2172G>T
(EGFR)
|
NP_001333826.1:p.Val724=
|
|
|
NM_001346898.2:c.2307G>T
(EGFR)
|
NP_001333827.1:p.Val769=
|
|
|
NM_001346900.2:c.2148G>T
(EGFR)
|
NP_001333829.1:p.Val716=
|
|
|
NM_001346941.2:c.1506G>T
(EGFR)
|
NP_001333870.1:p.Val502=
|
|
|
NM_001346899.2:c.2172G>T
(EGFR)
|
NP_001333828.1:p.Val724=
|
|
