ENST00000698420.1:c.*1095G>C
(TAP1)
|
ENSP00000513708.1:n.*1095G>C
|
|
ENST00000698421.1:c.*837G>C
(TAP1)
|
ENSP00000513709.1:n.*837G>C
|
|
ENST00000698422.1:c.1754G>C
(TAP1)
|
ENSP00000513710.1:p.Arg585Pro
|
|
ENST00000698423.1:c.1943G>C
(TAP1)
|
ENSP00000513711.1:p.Arg648Pro
|
|
ENST00000698424.1:c.1814G>C
(TAP1)
|
ENSP00000513712.1:p.Arg605Pro
|
|
ENST00000354258.5:c.1943G>C
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Arg648Pro
|
|
ENST00000643049.2:c.488G>C
(TAP1)
|
ENSP00000494148.2:p.Arg163Pro
|
|
ENST00000643923.1:n.1379G>C
(TAP1)
|
|
|
ENST00000645078.1:n.1538G>C
(TAP1)
|
|
|
ENST00000354258.4:c.2123G>C
(TAP1)
|
ENSP00000346206.4:p.Arg708Pro
|
|
ENST00000395330.5:c.-10+2891C>G
(PSMB9)
|
ENSP00000378739.1:n.-10+2891C>G
|
|
ENST00000414474.5:c.-10+2295C>G
(PSMB9)
|
ENSP00000394363.1:n.-10+2295C>G
|
|
ENST00000486332.1:n.1868G>C
(TAP1)
|
|
|
ENST00000487296.1:n.823G>C
(TAP1)
|
|
|
NM_000593.5:c.2123G>C
(TAP1)
|
NP_000584.2:p.Arg708Pro
|
|
NM_001292022.1:c.1340G>C
(TAP1)
|
NP_001278951.1:p.Arg447Pro
|
|
NM_001292022.2:c.1340G>C
(TAP1)
|
NP_001278951.1:p.Arg447Pro
|
|
NM_000593.6:c.1943G>C
(TAP1)
MANE Select
|
NP_000584.3:p.Arg648Pro
|
|