ENST00000698420.1:c.*1166G>T
(TAP1)
|
ENSP00000513708.1:n.*1166G>T
|
|
ENST00000698421.1:c.*908G>T
(TAP1)
|
ENSP00000513709.1:n.*908G>T
|
|
ENST00000698422.1:c.1825G>T
(TAP1)
|
ENSP00000513710.1:p.Ala609Ser
|
|
ENST00000698423.1:c.2014G>T
(TAP1)
|
ENSP00000513711.1:p.Ala672Ser
|
|
ENST00000698424.1:c.1885G>T
(TAP1)
|
ENSP00000513712.1:p.Ala629Ser
|
|
ENST00000354258.5:c.2014G>T
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Ala672Ser
|
|
ENST00000643049.2:c.559G>T
(TAP1)
|
ENSP00000494148.2:p.Ala187Ser
|
|
ENST00000643923.1:n.1450G>T
(TAP1)
|
|
|
ENST00000645078.1:n.1609G>T
(TAP1)
|
|
|
ENST00000354258.4:c.2194G>T
(TAP1)
|
ENSP00000346206.4:p.Ala732Ser
|
|
ENST00000395330.5:c.-10+2820C>A
(PSMB9)
|
ENSP00000378739.1:n.-10+2820C>A
|
|
ENST00000414474.5:c.-10+2224C>A
(PSMB9)
|
ENSP00000394363.1:n.-10+2224C>A
|
|
ENST00000486332.1:n.1939G>T
(TAP1)
|
|
|
ENST00000487296.1:n.894G>T
(TAP1)
|
|
|
NM_000593.5:c.2194G>T
(TAP1)
|
NP_000584.2:p.Ala732Ser
|
|
NM_001292022.1:c.1411G>T
(TAP1)
|
NP_001278951.1:p.Ala471Ser
|
|
NM_001292022.2:c.1411G>T
(TAP1)
|
NP_001278951.1:p.Ala471Ser
|
|
NM_000593.6:c.2014G>T
(TAP1)
MANE Select
|
NP_000584.3:p.Ala672Ser
|
|