ENST00000698420.1:c.*148G>C
(TAP1)
|
ENSP00000513708.1:n.*148G>C
|
|
ENST00000698421.1:c.845-481G>C
(TAP1)
|
ENSP00000513709.1:n.845-481G>C
|
|
ENST00000698422.1:c.996G>C
(TAP1)
|
ENSP00000513710.1:p.Leu332=
|
|
ENST00000698423.1:c.996G>C
(TAP1)
|
ENSP00000513711.1:p.Leu332=
|
|
ENST00000698424.1:c.996G>C
(TAP1)
|
ENSP00000513712.1:p.Leu332=
|
|
ENST00000354258.5:c.996G>C
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Leu332=
|
|
ENST00000643049.2:c.141+2498G>C
(TAP1)
|
ENSP00000494148.2:n.141+2498G>C
|
|
ENST00000643923.1:n.432G>C
(TAP1)
|
|
|
ENST00000645078.1:n.591G>C
(TAP1)
|
|
|
ENST00000354258.4:c.1176G>C
(TAP1)
|
ENSP00000346206.4:p.Leu392=
|
|
ENST00000395330.5:c.-9-5140C>G
(PSMB9)
|
ENSP00000378739.1:n.-9-5140C>G
|
|
ENST00000414474.5:c.-9-5140C>G
(PSMB9)
|
ENSP00000394363.1:n.-9-5140C>G
|
|
NM_000593.5:c.1176G>C
(TAP1)
|
NP_000584.2:p.Leu392=
|
|
NM_001292022.1:c.393G>C
(TAP1)
|
NP_001278951.1:p.Leu131=
|
|
NM_001292022.2:c.393G>C
(TAP1)
|
NP_001278951.1:p.Leu131=
|
|
NM_000593.6:c.996G>C
(TAP1)
MANE Select
|
NP_000584.3:p.Leu332=
|
|