ENST00000698420.1:c.*1058G>A
(TAP1)
|
ENSP00000513708.1:n.*1058G>A
|
|
ENST00000698421.1:c.*800G>A
(TAP1)
|
ENSP00000513709.1:n.*800G>A
|
|
ENST00000698422.1:c.1717G>A
(TAP1)
|
ENSP00000513710.1:p.Val573Ile
|
|
ENST00000698423.1:c.1906G>A
(TAP1)
|
ENSP00000513711.1:p.Val636Ile
|
|
ENST00000698424.1:c.1777G>A
(TAP1)
|
ENSP00000513712.1:p.Val593Ile
|
|
ENST00000354258.5:c.1906G>A
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Val636Ile
|
|
ENST00000643049.2:c.451G>A
(TAP1)
|
ENSP00000494148.2:p.Val151Ile
|
|
ENST00000643923.1:n.1342G>A
(TAP1)
|
|
|
ENST00000645078.1:n.1501G>A
(TAP1)
|
|
|
ENST00000354258.4:c.2086G>A
(TAP1)
|
ENSP00000346206.4:p.Val696Ile
|
|
ENST00000395330.5:c.-10+2928C>T
(PSMB9)
|
ENSP00000378739.1:n.-10+2928C>T
|
|
ENST00000414474.5:c.-10+2332C>T
(PSMB9)
|
ENSP00000394363.1:n.-10+2332C>T
|
|
ENST00000486332.1:n.1831G>A
(TAP1)
|
|
|
ENST00000487296.1:n.786G>A
(TAP1)
|
|
|
NM_000593.5:c.2086G>A
(TAP1)
|
NP_000584.2:p.Val696Ile
|
|
NM_001292022.1:c.1303G>A
(TAP1)
|
NP_001278951.1:p.Val435Ile
|
|
NM_001292022.2:c.1303G>A
(TAP1)
|
NP_001278951.1:p.Val435Ile
|
|
NM_000593.6:c.1906G>A
(TAP1)
MANE Select
|
NP_000584.3:p.Val636Ile
|
|