ENST00000698420.1:c.*1176C>G
(TAP1)
|
ENSP00000513708.1:n.*1176C>G
|
|
ENST00000698421.1:c.*918C>G
(TAP1)
|
ENSP00000513709.1:n.*918C>G
|
|
ENST00000698422.1:c.1835C>G
(TAP1)
|
ENSP00000513710.1:p.Ala612Gly
|
|
ENST00000698423.1:c.2024C>G
(TAP1)
|
ENSP00000513711.1:p.Ala675Gly
|
|
ENST00000698424.1:c.1895C>G
(TAP1)
|
ENSP00000513712.1:p.Ala632Gly
|
|
ENST00000354258.5:c.2024C>G
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Ala675Gly
|
|
ENST00000643049.2:c.569C>G
(TAP1)
|
ENSP00000494148.2:p.Ala190Gly
|
|
ENST00000643923.1:n.1460C>G
(TAP1)
|
|
|
ENST00000645078.1:n.1619C>G
(TAP1)
|
|
|
ENST00000354258.4:c.2204C>G
(TAP1)
|
ENSP00000346206.4:p.Ala735Gly
|
|
ENST00000395330.5:c.-10+2810G>C
(PSMB9)
|
ENSP00000378739.1:n.-10+2810G>C
|
|
ENST00000414474.5:c.-10+2214G>C
(PSMB9)
|
ENSP00000394363.1:n.-10+2214G>C
|
|
ENST00000486332.1:n.1949C>G
(TAP1)
|
|
|
ENST00000487296.1:n.904C>G
(TAP1)
|
|
|
NM_000593.5:c.2204C>G
(TAP1)
|
NP_000584.2:p.Ala735Gly
|
|
NM_001292022.1:c.1421C>G
(TAP1)
|
NP_001278951.1:p.Ala474Gly
|
|
NM_001292022.2:c.1421C>G
(TAP1)
|
NP_001278951.1:p.Ala474Gly
|
|
NM_000593.6:c.2024C>G
(TAP1)
MANE Select
|
NP_000584.3:p.Ala675Gly
|
|