ENST00000698420.1:c.*1091C>G
(TAP1)
|
ENSP00000513708.1:n.*1091C>G
|
|
ENST00000698421.1:c.*833C>G
(TAP1)
|
ENSP00000513709.1:n.*833C>G
|
|
ENST00000698422.1:c.1750C>G
(TAP1)
|
ENSP00000513710.1:p.Gln584Glu
|
|
ENST00000698423.1:c.1939C>G
(TAP1)
|
ENSP00000513711.1:p.Gln647Glu
|
|
ENST00000698424.1:c.1810C>G
(TAP1)
|
ENSP00000513712.1:p.Gln604Glu
|
|
ENST00000354258.5:c.1939C>G
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Gln647Glu
|
|
ENST00000643049.2:c.484C>G
(TAP1)
|
ENSP00000494148.2:p.Gln162Glu
|
|
ENST00000643923.1:n.1375C>G
(TAP1)
|
|
|
ENST00000645078.1:n.1534C>G
(TAP1)
|
|
|
ENST00000354258.4:c.2119C>G
(TAP1)
|
ENSP00000346206.4:p.Gln707Glu
|
|
ENST00000395330.5:c.-10+2895G>C
(PSMB9)
|
ENSP00000378739.1:n.-10+2895G>C
|
|
ENST00000414474.5:c.-10+2299G>C
(PSMB9)
|
ENSP00000394363.1:n.-10+2299G>C
|
|
ENST00000486332.1:n.1864C>G
(TAP1)
|
|
|
ENST00000487296.1:n.819C>G
(TAP1)
|
|
|
NM_000593.5:c.2119C>G
(TAP1)
|
NP_000584.2:p.Gln707Glu
|
|
NM_001292022.1:c.1336C>G
(TAP1)
|
NP_001278951.1:p.Gln446Glu
|
|
NM_001292022.2:c.1336C>G
(TAP1)
|
NP_001278951.1:p.Gln446Glu
|
|
NM_000593.6:c.1939C>G
(TAP1)
MANE Select
|
NP_000584.3:p.Gln647Glu
|
|