ENST00000347310.10:c.*178C>T
MANE Select
|
ENSP00000321345.5:n.*178C>T
|
|
ENST00000347310.9:c.*178C>T
|
ENSP00000321345.5:n.*178C>T
|
|
ENST00000395227.2:c.*178C>T
|
ENSP00000378652.2:n.*178C>T
|
|
ENST00000473881.2:c.*894C>T
|
ENSP00000486667.1:n.*894C>T
|
|
NM_144701.2:c.*178C>T
|
NP_653302.2:n.*178C>T
|
|
XM_005270516.2:c.*178C>T
|
XP_005270573.1:n.*178C>T
|
|
XM_011540789.1:c.*178C>T
|
XP_011539091.1:n.*178C>T
|
|
XM_011540790.1:c.*178C>T
|
XP_011539092.1:n.*178C>T
|
|
XM_011540791.1:c.*178C>T
|
XP_011539093.1:n.*178C>T
|
|
XM_011540790.3:c.*178C>T
|
XP_011539092.1:n.*178C>T
|
|
XM_011540791.3:c.*178C>T
|
XP_011539093.1:n.*178C>T
|
|
NM_144701.3:c.*178C>T
MANE Select
|
NP_653302.2:n.*178C>T
|
|