ENST00000647720.2:c.1517_1521delinsTCATC
(CFTR)
|
ENSP00000497673.2:p.Ile506=
|
|
ENST00000647978.2:c.*1231_*1235delinsTCATC
(CFTR)
|
ENSP00000497658.1:n.*1231_*1235delinsTCAT...
|
|
ENST00000649781.2:c.1334_1338delinsTCATC
(CFTR)
|
ENSP00000497203.1:p.Ile445=
|
|
ENST00000685018.2:c.1517_1521delinsTCATC
(CFTR)
|
ENSP00000510194.2:p.Ile506=
|
|
ENST00000687278.2:c.1517_1521delinsTCATC
(CFTR)
|
ENSP00000509593.2:p.Ile506=
|
|
ENST00000699585.1:c.1517_1521delinsTCATC
(CFTR)
|
ENSP00000514456.1:p.Ile506=
|
|
ENST00000699596.1:c.1517_1521delinsTCATC
(CFTR)
|
ENSP00000514465.1:p.Ile506=
|
|
ENST00000699597.1:c.*75_*79delinsTCATC
(CFTR)
|
ENSP00000514466.1:n.*75_*79delinsTCATC
|
|
ENST00000699598.1:c.1517_1521delinsTCATC
(CFTR)
|
ENSP00000514467.1:p.Ile506=
|
|
ENST00000699599.1:c.1517_1521delinsTCATC
(CFTR)
|
ENSP00000514468.1:p.Ile506=
|
|
ENST00000699600.1:c.1517_1521delinsTCATC
(CFTR)
|
ENSP00000514469.1:p.Ile506=
|
|
ENST00000699601.1:c.1517_1521delinsTCATC
(CFTR)
|
ENSP00000514470.1:p.Ile506=
|
|
ENST00000699602.1:c.1517_1521delinsTCATC
(CFTR)
|
ENSP00000514471.1:p.Ile506=
|
|
ENST00000699604.1:c.*1341_*1345delinsTCATC
(CFTR)
|
ENSP00000514472.1:n.*1341_*1345delinsTCAT...
|
|
ENST00000699605.1:c.1091_1095delinsTCATC
(CFTR)
|
ENSP00000514473.1:p.Ile364=
|
|
ENST00000003084.11:c.1517_1521delinsTCATC
(CFTR)
MANE Select
|
ENSP00000003084.6:p.Ile506=
|
|
ENST00000647978.1:c.*1231_*1235delinsTCATC
(CFTR)
|
ENSP00000497658.1:n.*1231_*1235delinsTCAT...
|
|
ENST00000648260.1:c.1334_1338delinsTCATC
(CFTR)
|
ENSP00000497957.1:p.Ile445=
|
|
ENST00000649406.1:c.1334_1338delinsTCATC
(CFTR)
|
ENSP00000497965.1:p.Ile445=
|
|
ENST00000649781.1:c.1334_1338delinsTCATC
(CFTR)
|
ENSP00000497203.1:p.Ile445=
|
|
ENST00000003084.10:c.1517_1521delinsTCATC
(CFTR)
|
ENSP00000003084.6:p.Ile506=
|
|
ENST00000426809.5:c.1427_1431delinsTCATC
(CFTR)
|
ENSP00000389119.1:p.Ile476=
|
|
NM_000492.3:c.1517_1521delinsTCATC , LRG_663t1:c.1517_1521delinsTCATC
(CFTR)
|
NP_000483.3:p.Ile506=
|
|
XM_011515751.1:c.1607_1611delinsTCATC
(CFTR)
|
XP_011514053.1:p.Ile536=
|
|
XM_011515752.1:c.1607_1611delinsTCATC
(CFTR)
|
XP_011514054.1:p.Ile536=
|
|
XM_011515753.1:c.1274_1278delinsTCATC
(CFTR)
|
XP_011514055.1:p.Ile425=
|
|
XM_011515754.1:c.1274_1278delinsTCATC
(CFTR)
|
XP_011514056.1:p.Ile425=
|
|
NR_149084.1:n.221+1141_221+1145delinsGATGA
(CFTR-AS1)
|
|
|
NM_000492.4:c.1517_1521delinsTCATC
(CFTR)
MANE Select
|
NP_000483.3:p.Ile506=
|
|