ENST00000403610.9:c.*442G>T
MANE Select
|
ENSP00000384604.3:n.*442G>T
|
|
ENST00000403610.8:c.*442G>T
|
ENSP00000384604.3:n.*442G>T
|
|
NM_001002919.2:c.*442G>T
|
NP_001002919.2:n.*442G>T
|
|
XM_005264689.3:c.*442G>T
|
XP_005264746.1:n.*442G>T
|
|
XM_006711879.2:c.*442G>T
|
XP_006711942.1:n.*442G>T
|
|
XM_006711881.2:c.*442G>T
|
XP_006711944.1:n.*442G>T
|
|
XM_011510342.1:c.*442G>T
|
XP_011508644.1:n.*442G>T
|
|
XM_005264689.5:c.*442G>T
|
XP_005264746.1:n.*442G>T
|
|
XM_006711879.4:c.*442G>T
|
XP_006711942.1:n.*442G>T
|
|
XM_011510342.3:c.*442G>T
|
XP_011508644.1:n.*442G>T
|
|
NM_001002919.3:c.*442G>T
MANE Select
|
NP_001002919.2:n.*442G>T
|
|