ENST00000698420.1:c.*1084A>T
(TAP1)
|
ENSP00000513708.1:n.*1084A>T
|
|
ENST00000698421.1:c.*826A>T
(TAP1)
|
ENSP00000513709.1:n.*826A>T
|
|
ENST00000698422.1:c.1743A>T
(TAP1)
|
ENSP00000513710.1:p.Ser581=
|
|
ENST00000698423.1:c.1932A>T
(TAP1)
|
ENSP00000513711.1:p.Ser644=
|
|
ENST00000698424.1:c.1803A>T
(TAP1)
|
ENSP00000513712.1:p.Ser601=
|
|
ENST00000354258.5:c.1932A>T
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Ser644=
|
|
ENST00000643049.2:c.477A>T
(TAP1)
|
ENSP00000494148.2:p.Ser159=
|
|
ENST00000643923.1:n.1368A>T
(TAP1)
|
|
|
ENST00000645078.1:n.1527A>T
(TAP1)
|
|
|
ENST00000354258.4:c.2112A>T
(TAP1)
|
ENSP00000346206.4:p.Ser704=
|
|
ENST00000395330.5:c.-10+2902T>A
(PSMB9)
|
ENSP00000378739.1:n.-10+2902T>A
|
|
ENST00000414474.5:c.-10+2306T>A
(PSMB9)
|
ENSP00000394363.1:n.-10+2306T>A
|
|
ENST00000486332.1:n.1857A>T
(TAP1)
|
|
|
ENST00000487296.1:n.812A>T
(TAP1)
|
|
|
NM_000593.5:c.2112A>T
(TAP1)
|
NP_000584.2:p.Ser704=
|
|
NM_001292022.1:c.1329A>T
(TAP1)
|
NP_001278951.1:p.Ser443=
|
|
NM_001292022.2:c.1329A>T
(TAP1)
|
NP_001278951.1:p.Ser443=
|
|
NM_000593.6:c.1932A>T
(TAP1)
MANE Select
|
NP_000584.3:p.Ser644=
|
|