ENST00000698420.1:c.*1170T>A
(TAP1)
|
ENSP00000513708.1:n.*1170T>A
|
|
ENST00000698421.1:c.*912T>A
(TAP1)
|
ENSP00000513709.1:n.*912T>A
|
|
ENST00000698422.1:c.1829T>A
(TAP1)
|
ENSP00000513710.1:p.Leu610Gln
|
|
ENST00000698423.1:c.2018T>A
(TAP1)
|
ENSP00000513711.1:p.Leu673Gln
|
|
ENST00000698424.1:c.1889T>A
(TAP1)
|
ENSP00000513712.1:p.Leu630Gln
|
|
ENST00000354258.5:c.2018T>A
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Leu673Gln
|
|
ENST00000643049.2:c.563T>A
(TAP1)
|
ENSP00000494148.2:p.Leu188Gln
|
|
ENST00000643923.1:n.1454T>A
(TAP1)
|
|
|
ENST00000645078.1:n.1613T>A
(TAP1)
|
|
|
ENST00000354258.4:c.2198T>A
(TAP1)
|
ENSP00000346206.4:p.Leu733Gln
|
|
ENST00000395330.5:c.-10+2816A>T
(PSMB9)
|
ENSP00000378739.1:n.-10+2816A>T
|
|
ENST00000414474.5:c.-10+2220A>T
(PSMB9)
|
ENSP00000394363.1:n.-10+2220A>T
|
|
ENST00000486332.1:n.1943T>A
(TAP1)
|
|
|
ENST00000487296.1:n.898T>A
(TAP1)
|
|
|
NM_000593.5:c.2198T>A
(TAP1)
|
NP_000584.2:p.Leu733Gln
|
|
NM_001292022.1:c.1415T>A
(TAP1)
|
NP_001278951.1:p.Leu472Gln
|
|
NM_001292022.2:c.1415T>A
(TAP1)
|
NP_001278951.1:p.Leu472Gln
|
|
NM_000593.6:c.2018T>A
(TAP1)
MANE Select
|
NP_000584.3:p.Leu673Gln
|
|