ENST00000394249.8:c.*949C>T
MANE Select
|
ENSP00000377793.3:n.*949C>T
|
|
ENST00000361188.9:c.*949C>T
|
ENSP00000354679.5:n.*949C>T
|
|
ENST00000394249.7:c.*949C>T
|
ENSP00000377793.3:n.*949C>T
|
|
ENST00000556972.6:c.596C>T
|
ENSP00000456737.1:n.596C>T
|
|
NM_001267580.1:c.*992C>T
|
NP_001254509.1:n.*992C>T
|
|
NM_003981.3:c.*949C>T
|
NP_003972.1:n.*949C>T
|
|
NM_199413.2:c.*949C>T
|
NP_955445.1:n.*949C>T
|
|
XM_005254987.1:c.*992C>T
|
XP_005255044.1:n.*992C>T
|
|
XM_006720759.1:c.*1043C>T
|
XP_006720822.1:n.*1043C>T
|
|
XM_006720760.1:c.*455C>T
|
XP_006720823.1:n.*455C>T
|
|
XM_011522187.1:c.*397C>T
|
XP_011520489.1:n.*397C>T
|
|
XM_011522188.1:c.*397C>T
|
XP_011520490.1:n.*397C>T
|
|
XM_011522189.1:c.*397C>T
|
XP_011520491.1:n.*397C>T
|
|
XM_011522190.1:c.*397C>T
|
XP_011520492.1:n.*397C>T
|
|
XM_011522192.1:c.*397C>T
|
XP_011520494.1:n.*397C>T
|
|
XM_005254987.3:c.*992C>T
|
XP_005255044.1:n.*992C>T
|
|
XM_006720759.2:c.*1043C>T
|
XP_006720822.1:n.*1043C>T
|
|
XM_006720760.2:c.*455C>T
|
XP_006720823.1:n.*455C>T
|
|
XM_011522187.2:c.*397C>T
|
XP_011520489.1:n.*397C>T
|
|
XM_011522188.3:c.*397C>T
|
XP_011520490.1:n.*397C>T
|
|
XM_011522189.2:c.*397C>T
|
XP_011520491.1:n.*397C>T
|
|
XM_011522191.3:c.*494C>T
|
XP_011520493.1:n.*494C>T
|
|
XM_011522192.2:c.*397C>T
|
XP_011520494.1:n.*397C>T
|
|
XM_017022712.2:c.*949C>T
|
XP_016878201.1:n.*949C>T
|
|
XM_017022713.2:c.*949C>T
|
XP_016878202.1:n.*949C>T
|
|
XM_017022715.2:c.*949C>T
|
XP_016878204.1:n.*949C>T
|
|
XM_017022716.2:c.*949C>T
|
XP_016878205.1:n.*949C>T
|
|
XM_017022717.1:c.*992C>T
|
XP_016878206.1:n.*992C>T
|
|
NM_003981.4:c.*949C>T
MANE Select
|
NP_003972.2:n.*949C>T
|
|
NM_001267580.2:c.*992C>T
|
NP_001254509.2:n.*992C>T
|
|
NM_199413.3:c.*949C>T
|
NP_955445.2:n.*949C>T
|
|