ENST00000698420.1:c.*1163A>C
(TAP1)
|
ENSP00000513708.1:n.*1163A>C
|
|
ENST00000698421.1:c.*905A>C
(TAP1)
|
ENSP00000513709.1:n.*905A>C
|
|
ENST00000698422.1:c.1822A>C
(TAP1)
|
ENSP00000513710.1:p.Ser608Arg
|
|
ENST00000698423.1:c.2011A>C
(TAP1)
|
ENSP00000513711.1:p.Ser671Arg
|
|
ENST00000698424.1:c.1882A>C
(TAP1)
|
ENSP00000513712.1:p.Ser628Arg
|
|
ENST00000354258.5:c.2011A>C
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Ser671Arg
|
|
ENST00000643049.2:c.556A>C
(TAP1)
|
ENSP00000494148.2:p.Ser186Arg
|
|
ENST00000643923.1:n.1447A>C
(TAP1)
|
|
|
ENST00000645078.1:n.1606A>C
(TAP1)
|
|
|
ENST00000354258.4:c.2191A>C
(TAP1)
|
ENSP00000346206.4:p.Ser731Arg
|
|
ENST00000395330.5:c.-10+2823T>G
(PSMB9)
|
ENSP00000378739.1:n.-10+2823T>G
|
|
ENST00000414474.5:c.-10+2227T>G
(PSMB9)
|
ENSP00000394363.1:n.-10+2227T>G
|
|
ENST00000486332.1:n.1936A>C
(TAP1)
|
|
|
ENST00000487296.1:n.891A>C
(TAP1)
|
|
|
NM_000593.5:c.2191A>C
(TAP1)
|
NP_000584.2:p.Ser731Arg
|
|
NM_001292022.1:c.1408A>C
(TAP1)
|
NP_001278951.1:p.Ser470Arg
|
|
NM_001292022.2:c.1408A>C
(TAP1)
|
NP_001278951.1:p.Ser470Arg
|
|
NM_000593.6:c.2011A>C
(TAP1)
MANE Select
|
NP_000584.3:p.Ser671Arg
|
|