ENST00000698420.1:c.*1057G>C
(TAP1)
|
ENSP00000513708.1:n.*1057G>C
|
|
ENST00000698421.1:c.*799G>C
(TAP1)
|
ENSP00000513709.1:n.*799G>C
|
|
ENST00000698422.1:c.1716G>C
(TAP1)
|
ENSP00000513710.1:p.Glu572Asp
|
|
ENST00000698423.1:c.1905G>C
(TAP1)
|
ENSP00000513711.1:p.Glu635Asp
|
|
ENST00000698424.1:c.1776G>C
(TAP1)
|
ENSP00000513712.1:p.Glu592Asp
|
|
ENST00000354258.5:c.1905G>C
(TAP1)
MANE Select
|
ENSP00000346206.5:p.Glu635Asp
|
|
ENST00000643049.2:c.450G>C
(TAP1)
|
ENSP00000494148.2:p.Glu150Asp
|
|
ENST00000643923.1:n.1341G>C
(TAP1)
|
|
|
ENST00000645078.1:n.1500G>C
(TAP1)
|
|
|
ENST00000354258.4:c.2085G>C
(TAP1)
|
ENSP00000346206.4:p.Glu695Asp
|
|
ENST00000395330.5:c.-10+2929C>G
(PSMB9)
|
ENSP00000378739.1:n.-10+2929C>G
|
|
ENST00000414474.5:c.-10+2333C>G
(PSMB9)
|
ENSP00000394363.1:n.-10+2333C>G
|
|
ENST00000486332.1:n.1830G>C
(TAP1)
|
|
|
ENST00000487296.1:n.785G>C
(TAP1)
|
|
|
NM_000593.5:c.2085G>C
(TAP1)
|
NP_000584.2:p.Glu695Asp
|
|
NM_001292022.1:c.1302G>C
(TAP1)
|
NP_001278951.1:p.Glu434Asp
|
|
NM_001292022.2:c.1302G>C
(TAP1)
|
NP_001278951.1:p.Glu434Asp
|
|
NM_000593.6:c.1905G>C
(TAP1)
MANE Select
|
NP_000584.3:p.Glu635Asp
|
|