|
ENST00000358647.5:c.*498G>T
(GIMAP5)
MANE Select
|
ENSP00000351473.3:n.*498G>T
|
|
|
ENST00000358647.4:c.*498G>T
(GIMAP5)
|
ENSP00000351473.3:n.*498G>T
|
|
|
ENST00000466347.5:n.131+2634G>T
(GIMAP5)
|
|
|
|
ENST00000476324.1:n.4697G>T
(GIMAP5)
|
|
|
|
ENST00000479556.1:n.1470G>T
(GIMAP5)
|
|
|
|
ENST00000498181.6:c.*498G>T
(GIMAP5)
|
ENSP00000487840.2:n.*498G>T
|
|
|
ENST00000611999.4:c.*498G>T
(GIMAP1-GIMAP5)
|
ENSP00000477920.1:n.*498G>T
|
|
|
NM_001199577.1:c.*498G>T
(GIMAP1-GIMAP5)
|
NP_001186506.1:n.*498G>T
|
|
|
NM_001303630.1:c.*498G>T
(GIMAP1-GIMAP5)
|
NP_001290559.1:n.*498G>T
|
|
|
NM_018384.4:c.*498G>T
(GIMAP5)
|
NP_060854.2:n.*498G>T
|
|
|
NM_001199577.2:c.*498G>T
(GIMAP1-GIMAP5)
|
NP_001186506.1:n.*498G>T
|
|
|
NM_001303630.2:c.*498G>T
(GIMAP1-GIMAP5)
|
NP_001290559.1:n.*498G>T
|
|
|
NM_018384.5:c.*498G>T
(GIMAP5)
MANE Select
|
NP_060854.2:n.*498G>T
|
|
