ENST00000698420.1:c.*1182G>C
(TAP1)
|
ENSP00000513708.1:n.*1182G>C
|
|
ENST00000698421.1:c.*924G>C
(TAP1)
|
ENSP00000513709.1:n.*924G>C
|
|
ENST00000698422.1:c.1841G>C
(TAP1)
|
ENSP00000513710.1:p.Ser614Thr
|
|
ENST00000698423.1:c.2030G>C
(TAP1)
|
ENSP00000513711.1:p.Ser677Thr
|
|
ENST00000698424.1:c.1901G>C
(TAP1)
|
ENSP00000513712.1:p.Ser634Thr
|
|
ENST00000354258.5:c.2030G>C
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Ser677Thr
|
|
ENST00000643049.2:c.575G>C
(TAP1)
|
ENSP00000494148.2:p.Ser192Thr
|
|
ENST00000643923.1:n.1466G>C
(TAP1)
|
|
|
ENST00000645078.1:n.1625G>C
(TAP1)
|
|
|
ENST00000354258.4:c.2210G>C
(TAP1)
|
ENSP00000346206.4:p.Ser737Thr
|
|
ENST00000395330.5:c.-10+2804C>G
(PSMB9)
|
ENSP00000378739.1:n.-10+2804C>G
|
|
ENST00000414474.5:c.-10+2208C>G
(PSMB9)
|
ENSP00000394363.1:n.-10+2208C>G
|
|
ENST00000486332.1:n.1955G>C
(TAP1)
|
|
|
ENST00000487296.1:n.910G>C
(TAP1)
|
|
|
NM_000593.5:c.2210G>C
(TAP1)
|
NP_000584.2:p.Ser737Thr
|
|
NM_001292022.1:c.1427G>C
(TAP1)
|
NP_001278951.1:p.Ser476Thr
|
|
NM_001292022.2:c.1427G>C
(TAP1)
|
NP_001278951.1:p.Ser476Thr
|
|
NM_000593.6:c.2030G>C
(TAP1)
MANE Select
|
NP_000584.3:p.Ser677Thr
|
|