ENST00000369458.8:c.*43C>T
MANE Select
|
ENSP00000358470.3:n.*43C>T
|
|
ENST00000328189.7:c.*43C>T
|
ENSP00000328168.3:n.*43C>T
|
|
ENST00000359008.8:c.*43C>T
|
ENSP00000351899.4:n.*43C>T
|
|
ENST00000369458.7:c.*43C>T
|
ENSP00000358470.3:n.*43C>T
|
|
ENST00000539893.5:c.*43C>T
|
ENSP00000444724.1:n.*43C>T
|
|
NM_001253849.1:c.*43C>T
|
NP_001240778.1:n.*43C>T
|
|
NM_001253850.1:c.*43C>T
|
NP_001240779.1:n.*43C>T
|
|
NM_024626.3:c.*43C>T
|
NP_078902.2:n.*43C>T
|
|
NR_045603.1:n.1087C>T
|
|
|
NR_045604.1:n.791C>T
|
|
|
XM_011542143.1:c.*43C>T
|
XP_011540445.1:n.*43C>T
|
|
XM_011542144.1:c.*43C>T
|
XP_011540446.1:n.*43C>T
|
|
XM_011542145.1:c.*43C>T
|
XP_011540447.1:n.*43C>T
|
|
XM_011542143.2:c.*43C>T
|
XP_011540445.2:n.*43C>T
|
|
XM_017002335.2:c.*43C>T
|
XP_016857824.1:n.*43C>T
|
|
NM_024626.4:c.*43C>T
MANE Select
|
NP_078902.2:n.*43C>T
|
|
NR_045603.2:n.1054C>T
|
|
|
NR_045604.2:n.758C>T
|
|
|
NM_001253849.2:c.*43C>T
|
NP_001240778.1:n.*43C>T
|
|
NM_001253850.2:c.*43C>T
|
NP_001240779.1:n.*43C>T
|
|