ENST00000698420.1:c.*1089G>C
(TAP1)
|
ENSP00000513708.1:n.*1089G>C
|
|
ENST00000698421.1:c.*831G>C
(TAP1)
|
ENSP00000513709.1:n.*831G>C
|
|
ENST00000698422.1:c.1748G>C
(TAP1)
|
ENSP00000513710.1:p.Gly583Ala
|
|
ENST00000698423.1:c.1937G>C
(TAP1)
|
ENSP00000513711.1:p.Gly646Ala
|
|
ENST00000698424.1:c.1808G>C
(TAP1)
|
ENSP00000513712.1:p.Gly603Ala
|
|
ENST00000354258.5:c.1937G>C
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Gly646Ala
|
|
ENST00000643049.2:c.482G>C
(TAP1)
|
ENSP00000494148.2:p.Gly161Ala
|
|
ENST00000643923.1:n.1373G>C
(TAP1)
|
|
|
ENST00000645078.1:n.1532G>C
(TAP1)
|
|
|
ENST00000354258.4:c.2117G>C
(TAP1)
|
ENSP00000346206.4:p.Gly706Ala
|
|
ENST00000395330.5:c.-10+2897C>G
(PSMB9)
|
ENSP00000378739.1:n.-10+2897C>G
|
|
ENST00000414474.5:c.-10+2301C>G
(PSMB9)
|
ENSP00000394363.1:n.-10+2301C>G
|
|
ENST00000486332.1:n.1862G>C
(TAP1)
|
|
|
ENST00000487296.1:n.817G>C
(TAP1)
|
|
|
NM_000593.5:c.2117G>C
(TAP1)
|
NP_000584.2:p.Gly706Ala
|
|
NM_001292022.1:c.1334G>C
(TAP1)
|
NP_001278951.1:p.Gly445Ala
|
|
NM_001292022.2:c.1334G>C
(TAP1)
|
NP_001278951.1:p.Gly445Ala
|
|
NM_000593.6:c.1937G>C
(TAP1)
MANE Select
|
NP_000584.3:p.Gly646Ala
|
|