ENST00000401061.9:c.*1738G>A
(MMACHC)
MANE Select
|
ENSP00000383840.4:n.*1738G>A
|
|
ENST00000424390.2:c.*376C>T
(PRDX1)
|
ENSP00000389047.2:n.*376C>T
|
|
ENST00000447184.6:c.*376C>T
(PRDX1)
|
ENSP00000407034.2:n.*376C>T
|
|
ENST00000676549.1:c.*376C>T
(PRDX1)
|
ENSP00000503140.1:n.*376C>T
|
|
ENST00000401061.8:c.*1738G>A
(MMACHC)
|
ENSP00000383840.4:n.*1738G>A
|
|
ENST00000616135.1:c.*557G>A
(MMACHC)
|
ENSP00000478859.1:n.*557G>A
|
|
NM_015506.2:c.*1738G>A
(MMACHC)
|
NP_056321.2:n.*1738G>A
|
|
NM_001330540.1:c.*1738G>A
(MMACHC)
|
NP_001317469.1:n.*1738G>A
|
|
XM_005270724.5:c.*1738G>A
(MMACHC)
|
XP_005270781.1:n.*1738G>A
|
|
NM_015506.3:c.*1738G>A
(MMACHC)
MANE Select
|
NP_056321.2:n.*1738G>A
|
|
NM_001330540.2:c.*1738G>A
(MMACHC)
|
NP_001317469.1:n.*1738G>A
|
|