ENST00000698420.1:c.*1164G>T
(TAP1)
|
ENSP00000513708.1:n.*1164G>T
|
|
ENST00000698421.1:c.*906G>T
(TAP1)
|
ENSP00000513709.1:n.*906G>T
|
|
ENST00000698422.1:c.1823G>T
(TAP1)
|
ENSP00000513710.1:p.Ser608Ile
|
|
ENST00000698423.1:c.2012G>T
(TAP1)
|
ENSP00000513711.1:p.Ser671Ile
|
|
ENST00000698424.1:c.1883G>T
(TAP1)
|
ENSP00000513712.1:p.Ser628Ile
|
|
ENST00000354258.5:c.2012G>T
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Ser671Ile
|
|
ENST00000643049.2:c.557G>T
(TAP1)
|
ENSP00000494148.2:p.Ser186Ile
|
|
ENST00000643923.1:n.1448G>T
(TAP1)
|
|
|
ENST00000645078.1:n.1607G>T
(TAP1)
|
|
|
ENST00000354258.4:c.2192G>T
(TAP1)
|
ENSP00000346206.4:p.Ser731Ile
|
|
ENST00000395330.5:c.-10+2822C>A
(PSMB9)
|
ENSP00000378739.1:n.-10+2822C>A
|
|
ENST00000414474.5:c.-10+2226C>A
(PSMB9)
|
ENSP00000394363.1:n.-10+2226C>A
|
|
ENST00000486332.1:n.1937G>T
(TAP1)
|
|
|
ENST00000487296.1:n.892G>T
(TAP1)
|
|
|
NM_000593.5:c.2192G>T
(TAP1)
|
NP_000584.2:p.Ser731Ile
|
|
NM_001292022.1:c.1409G>T
(TAP1)
|
NP_001278951.1:p.Ser470Ile
|
|
NM_001292022.2:c.1409G>T
(TAP1)
|
NP_001278951.1:p.Ser470Ile
|
|
NM_000593.6:c.2012G>T
(TAP1)
MANE Select
|
NP_000584.3:p.Ser671Ile
|
|