ENST00000698420.1:c.*1159C>T
(TAP1)
|
ENSP00000513708.1:n.*1159C>T
|
|
ENST00000698421.1:c.*901C>T
(TAP1)
|
ENSP00000513709.1:n.*901C>T
|
|
ENST00000698422.1:c.1818C>T
(TAP1)
|
ENSP00000513710.1:p.Ala606=
|
|
ENST00000698423.1:c.2007C>T
(TAP1)
|
ENSP00000513711.1:p.Ala669=
|
|
ENST00000698424.1:c.1878C>T
(TAP1)
|
ENSP00000513712.1:p.Ala626=
|
|
ENST00000354258.5:c.2007C>T
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Ala669=
|
|
ENST00000643049.2:c.552C>T
(TAP1)
|
ENSP00000494148.2:p.Ala184=
|
|
ENST00000643923.1:n.1443C>T
(TAP1)
|
|
|
ENST00000645078.1:n.1602C>T
(TAP1)
|
|
|
ENST00000354258.4:c.2187C>T
(TAP1)
|
ENSP00000346206.4:p.Ala729=
|
|
ENST00000395330.5:c.-10+2827G>A
(PSMB9)
|
ENSP00000378739.1:n.-10+2827G>A
|
|
ENST00000414474.5:c.-10+2231G>A
(PSMB9)
|
ENSP00000394363.1:n.-10+2231G>A
|
|
ENST00000486332.1:n.1932C>T
(TAP1)
|
|
|
ENST00000487296.1:n.887C>T
(TAP1)
|
|
|
NM_000593.5:c.2187C>T
(TAP1)
|
NP_000584.2:p.Ala729=
|
|
NM_001292022.1:c.1404C>T
(TAP1)
|
NP_001278951.1:p.Ala468=
|
|
NM_001292022.2:c.1404C>T
(TAP1)
|
NP_001278951.1:p.Ala468=
|
|
NM_000593.6:c.2007C>T
(TAP1)
MANE Select
|
NP_000584.3:p.Ala669=
|
|