ENST00000698420.1:c.*141T>G
(TAP1)
|
ENSP00000513708.1:n.*141T>G
|
|
ENST00000698421.1:c.845-488T>G
(TAP1)
|
ENSP00000513709.1:n.845-488T>G
|
|
ENST00000698422.1:c.989T>G
(TAP1)
|
ENSP00000513710.1:p.Val330Gly
|
|
ENST00000698423.1:c.989T>G
(TAP1)
|
ENSP00000513711.1:p.Val330Gly
|
|
ENST00000698424.1:c.989T>G
(TAP1)
|
ENSP00000513712.1:p.Val330Gly
|
|
ENST00000354258.5:c.989T>G
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Val330Gly
|
|
ENST00000643049.2:c.141+2491T>G
(TAP1)
|
ENSP00000494148.2:n.141+2491T>G
|
|
ENST00000643923.1:n.425T>G
(TAP1)
|
|
|
ENST00000645078.1:n.584T>G
(TAP1)
|
|
|
ENST00000354258.4:c.1169T>G
(TAP1)
|
ENSP00000346206.4:p.Val390Gly
|
|
ENST00000395330.5:c.-9-5133A>C
(PSMB9)
|
ENSP00000378739.1:n.-9-5133A>C
|
|
ENST00000414474.5:c.-9-5133A>C
(PSMB9)
|
ENSP00000394363.1:n.-9-5133A>C
|
|
NM_000593.5:c.1169T>G
(TAP1)
|
NP_000584.2:p.Val390Gly
|
|
NM_001292022.1:c.386T>G
(TAP1)
|
NP_001278951.1:p.Val129Gly
|
|
NM_001292022.2:c.386T>G
(TAP1)
|
NP_001278951.1:p.Val129Gly
|
|
NM_000593.6:c.989T>G
(TAP1)
MANE Select
|
NP_000584.3:p.Val330Gly
|
|