ENST00000698420.1:c.*1162C>G
(TAP1)
|
ENSP00000513708.1:n.*1162C>G
|
|
ENST00000698421.1:c.*904C>G
(TAP1)
|
ENSP00000513709.1:n.*904C>G
|
|
ENST00000698422.1:c.1821C>G
(TAP1)
|
ENSP00000513710.1:p.Thr607=
|
|
ENST00000698423.1:c.2010C>G
(TAP1)
|
ENSP00000513711.1:p.Thr670=
|
|
ENST00000698424.1:c.1881C>G
(TAP1)
|
ENSP00000513712.1:p.Thr627=
|
|
ENST00000354258.5:c.2010C>G
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Thr670=
|
|
ENST00000643049.2:c.555C>G
(TAP1)
|
ENSP00000494148.2:p.Thr185=
|
|
ENST00000643923.1:n.1446C>G
(TAP1)
|
|
|
ENST00000645078.1:n.1605C>G
(TAP1)
|
|
|
ENST00000354258.4:c.2190C>G
(TAP1)
|
ENSP00000346206.4:p.Thr730=
|
|
ENST00000395330.5:c.-10+2824G>C
(PSMB9)
|
ENSP00000378739.1:n.-10+2824G>C
|
|
ENST00000414474.5:c.-10+2228G>C
(PSMB9)
|
ENSP00000394363.1:n.-10+2228G>C
|
|
ENST00000486332.1:n.1935C>G
(TAP1)
|
|
|
ENST00000487296.1:n.890C>G
(TAP1)
|
|
|
NM_000593.5:c.2190C>G
(TAP1)
|
NP_000584.2:p.Thr730=
|
|
NM_001292022.1:c.1407C>G
(TAP1)
|
NP_001278951.1:p.Thr469=
|
|
NM_001292022.2:c.1407C>G
(TAP1)
|
NP_001278951.1:p.Thr469=
|
|
NM_000593.6:c.2010C>G
(TAP1)
MANE Select
|
NP_000584.3:p.Thr670=
|
|