ENST00000698420.1:c.*1148C>G
(TAP1)
|
ENSP00000513708.1:n.*1148C>G
|
|
ENST00000698421.1:c.*890C>G
(TAP1)
|
ENSP00000513709.1:n.*890C>G
|
|
ENST00000698422.1:c.1807C>G
(TAP1)
|
ENSP00000513710.1:p.Leu603Val
|
|
ENST00000698423.1:c.1996C>G
(TAP1)
|
ENSP00000513711.1:p.Leu666Val
|
|
ENST00000698424.1:c.1867C>G
(TAP1)
|
ENSP00000513712.1:p.Leu623Val
|
|
ENST00000354258.5:c.1996C>G
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Leu666Val
|
|
ENST00000643049.2:c.541C>G
(TAP1)
|
ENSP00000494148.2:p.Leu181Val
|
|
ENST00000643923.1:n.1432C>G
(TAP1)
|
|
|
ENST00000645078.1:n.1591C>G
(TAP1)
|
|
|
ENST00000354258.4:c.2176C>G
(TAP1)
|
ENSP00000346206.4:p.Leu726Val
|
|
ENST00000395330.5:c.-10+2838G>C
(PSMB9)
|
ENSP00000378739.1:n.-10+2838G>C
|
|
ENST00000414474.5:c.-10+2242G>C
(PSMB9)
|
ENSP00000394363.1:n.-10+2242G>C
|
|
ENST00000486332.1:n.1921C>G
(TAP1)
|
|
|
ENST00000487296.1:n.876C>G
(TAP1)
|
|
|
NM_000593.5:c.2176C>G
(TAP1)
|
NP_000584.2:p.Leu726Val
|
|
NM_001292022.1:c.1393C>G
(TAP1)
|
NP_001278951.1:p.Leu465Val
|
|
NM_001292022.2:c.1393C>G
(TAP1)
|
NP_001278951.1:p.Leu465Val
|
|
NM_000593.6:c.1996C>G
(TAP1)
MANE Select
|
NP_000584.3:p.Leu666Val
|
|