ENST00000698420.1:c.*1168C>G
(TAP1)
|
ENSP00000513708.1:n.*1168C>G
|
|
ENST00000698421.1:c.*910C>G
(TAP1)
|
ENSP00000513709.1:n.*910C>G
|
|
ENST00000698422.1:c.1827C>G
(TAP1)
|
ENSP00000513710.1:p.Ala609=
|
|
ENST00000698423.1:c.2016C>G
(TAP1)
|
ENSP00000513711.1:p.Ala672=
|
|
ENST00000698424.1:c.1887C>G
(TAP1)
|
ENSP00000513712.1:p.Ala629=
|
|
ENST00000354258.5:c.2016C>G
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Ala672=
|
|
ENST00000643049.2:c.561C>G
(TAP1)
|
ENSP00000494148.2:p.Ala187=
|
|
ENST00000643923.1:n.1452C>G
(TAP1)
|
|
|
ENST00000645078.1:n.1611C>G
(TAP1)
|
|
|
ENST00000354258.4:c.2196C>G
(TAP1)
|
ENSP00000346206.4:p.Ala732=
|
|
ENST00000395330.5:c.-10+2818G>C
(PSMB9)
|
ENSP00000378739.1:n.-10+2818G>C
|
|
ENST00000414474.5:c.-10+2222G>C
(PSMB9)
|
ENSP00000394363.1:n.-10+2222G>C
|
|
ENST00000486332.1:n.1941C>G
(TAP1)
|
|
|
ENST00000487296.1:n.896C>G
(TAP1)
|
|
|
NM_000593.5:c.2196C>G
(TAP1)
|
NP_000584.2:p.Ala732=
|
|
NM_001292022.1:c.1413C>G
(TAP1)
|
NP_001278951.1:p.Ala471=
|
|
NM_001292022.2:c.1413C>G
(TAP1)
|
NP_001278951.1:p.Ala471=
|
|
NM_000593.6:c.2016C>G
(TAP1)
MANE Select
|
NP_000584.3:p.Ala672=
|
|