ENST00000698420.1:c.*1192G>T
(TAP1)
|
ENSP00000513708.1:n.*1192G>T
|
|
ENST00000698421.1:c.*934G>T
(TAP1)
|
ENSP00000513709.1:n.*934G>T
|
|
ENST00000698422.1:c.1851G>T
(TAP1)
|
ENSP00000513710.1:p.Gln617His
|
|
ENST00000698423.1:c.2040G>T
(TAP1)
|
ENSP00000513711.1:p.Gln680His
|
|
ENST00000698424.1:c.1911G>T
(TAP1)
|
ENSP00000513712.1:p.Gln637His
|
|
ENST00000354258.5:c.2040G>T
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Gln680His
|
|
ENST00000643049.2:c.585G>T
(TAP1)
|
ENSP00000494148.2:p.Gln195His
|
|
ENST00000643923.1:n.1476G>T
(TAP1)
|
|
|
ENST00000645078.1:n.1635G>T
(TAP1)
|
|
|
ENST00000354258.4:c.2220G>T
(TAP1)
|
ENSP00000346206.4:p.Gln740His
|
|
ENST00000395330.5:c.-10+2794C>A
(PSMB9)
|
ENSP00000378739.1:n.-10+2794C>A
|
|
ENST00000414474.5:c.-10+2198C>A
(PSMB9)
|
ENSP00000394363.1:n.-10+2198C>A
|
|
ENST00000486332.1:n.1965G>T
(TAP1)
|
|
|
ENST00000487296.1:n.920G>T
(TAP1)
|
|
|
NM_000593.5:c.2220G>T
(TAP1)
|
NP_000584.2:p.Gln740His
|
|
NM_001292022.1:c.1437G>T
(TAP1)
|
NP_001278951.1:p.Gln479His
|
|
NM_001292022.2:c.1437G>T
(TAP1)
|
NP_001278951.1:p.Gln479His
|
|
NM_000593.6:c.2040G>T
(TAP1)
MANE Select
|
NP_000584.3:p.Gln680His
|
|