ENST00000698420.1:c.*1177A>C
(TAP1)
|
ENSP00000513708.1:n.*1177A>C
|
|
ENST00000698421.1:c.*919A>C
(TAP1)
|
ENSP00000513709.1:n.*919A>C
|
|
ENST00000698422.1:c.1836A>C
(TAP1)
|
ENSP00000513710.1:p.Ala612=
|
|
ENST00000698423.1:c.2025A>C
(TAP1)
|
ENSP00000513711.1:p.Ala675=
|
|
ENST00000698424.1:c.1896A>C
(TAP1)
|
ENSP00000513712.1:p.Ala632=
|
|
ENST00000354258.5:c.2025A>C
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Ala675=
|
|
ENST00000643049.2:c.570A>C
(TAP1)
|
ENSP00000494148.2:p.Ala190=
|
|
ENST00000643923.1:n.1461A>C
(TAP1)
|
|
|
ENST00000645078.1:n.1620A>C
(TAP1)
|
|
|
ENST00000354258.4:c.2205A>C
(TAP1)
|
ENSP00000346206.4:p.Ala735=
|
|
ENST00000395330.5:c.-10+2809T>G
(PSMB9)
|
ENSP00000378739.1:n.-10+2809T>G
|
|
ENST00000414474.5:c.-10+2213T>G
(PSMB9)
|
ENSP00000394363.1:n.-10+2213T>G
|
|
ENST00000486332.1:n.1950A>C
(TAP1)
|
|
|
ENST00000487296.1:n.905A>C
(TAP1)
|
|
|
NM_000593.5:c.2205A>C
(TAP1)
|
NP_000584.2:p.Ala735=
|
|
NM_001292022.1:c.1422A>C
(TAP1)
|
NP_001278951.1:p.Ala474=
|
|
NM_001292022.2:c.1422A>C
(TAP1)
|
NP_001278951.1:p.Ala474=
|
|
NM_000593.6:c.2025A>C
(TAP1)
MANE Select
|
NP_000584.3:p.Ala675=
|
|