ENST00000312251.8:c.982C>T
MANE Select
|
ENSP00000310998.3:p.Arg328Cys
|
|
ENST00000649828.1:c.*154C>T
|
ENSP00000498032.1:n.*154C>T
|
|
ENST00000312251.7:c.982C>T
|
ENSP00000310998.3:p.Arg328Cys
|
|
ENST00000381955.7:c.982C>T
|
ENSP00000371381.3:p.Arg328Cys
|
|
ENST00000562346.2:c.566C>T
|
|
|
ENST00000562746.5:c.*154C>T
|
ENSP00000455900.1:n.*154C>T
|
|
ENST00000563578.5:c.738+756C>T
|
|
|
ENST00000564397.5:n.2035C>T
|
|
|
ENST00000565876.5:c.481-745C>T
|
|
|
ENST00000566137.5:n.280C>T
|
|
|
ENST00000567739.5:n.301C>T
|
|
|
ENST00000568202.5:n.845C>T
|
|
|
ENST00000568528.1:n.491C>T
|
|
|
ENST00000569296.5:c.595C>T
|
ENSP00000465949.1:n.595C>T
|
|
NM_016256.3:c.982C>T
|
NP_057340.2:p.Arg328Cys
|
|
XM_011522517.1:c.982C>T
|
XP_011520819.1:p.Arg328Cys
|
|
XM_011522518.1:c.*80C>T
|
XP_011520820.1:n.*80C>T
|
|
XR_243285.1:n.1078C>T
|
|
|
XM_011522517.3:c.982C>T
|
XP_011520819.1:p.Arg328Cys
|
|
XR_001751908.2:n.1077C>T
|
|
|
XR_001751909.2:n.1081C>T
|
|
|
XR_001751910.2:n.1110C>T
|
|
|
XR_001751911.2:n.1110C>T
|
|
|
XR_001751912.2:n.1114C>T
|
|
|
NM_016256.4:c.982C>T
MANE Select
|
NP_057340.2:p.Arg328Cys
|
|