ENST00000698420.1:c.*1154G>C
(TAP1)
|
ENSP00000513708.1:n.*1154G>C
|
|
ENST00000698421.1:c.*896G>C
(TAP1)
|
ENSP00000513709.1:n.*896G>C
|
|
ENST00000698422.1:c.1813G>C
(TAP1)
|
ENSP00000513710.1:p.Asp605His
|
|
ENST00000698423.1:c.2002G>C
(TAP1)
|
ENSP00000513711.1:p.Asp668His
|
|
ENST00000698424.1:c.1873G>C
(TAP1)
|
ENSP00000513712.1:p.Asp625His
|
|
ENST00000354258.5:c.2002G>C
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Asp668His
|
|
ENST00000643049.2:c.547G>C
(TAP1)
|
ENSP00000494148.2:p.Asp183His
|
|
ENST00000643923.1:n.1438G>C
(TAP1)
|
|
|
ENST00000645078.1:n.1597G>C
(TAP1)
|
|
|
ENST00000354258.4:c.2182G>C
(TAP1)
|
ENSP00000346206.4:p.Asp728His
|
|
ENST00000395330.5:c.-10+2832C>G
(PSMB9)
|
ENSP00000378739.1:n.-10+2832C>G
|
|
ENST00000414474.5:c.-10+2236C>G
(PSMB9)
|
ENSP00000394363.1:n.-10+2236C>G
|
|
ENST00000486332.1:n.1927G>C
(TAP1)
|
|
|
ENST00000487296.1:n.882G>C
(TAP1)
|
|
|
NM_000593.5:c.2182G>C
(TAP1)
|
NP_000584.2:p.Asp728His
|
|
NM_001292022.1:c.1399G>C
(TAP1)
|
NP_001278951.1:p.Asp467His
|
|
NM_001292022.2:c.1399G>C
(TAP1)
|
NP_001278951.1:p.Asp467His
|
|
NM_000593.6:c.2002G>C
(TAP1)
MANE Select
|
NP_000584.3:p.Asp668His
|
|