ENST00000313468.10:c.196C>T
MANE Select
|
ENSP00000315774.5:p.Arg66Ter
|
|
ENST00000313468.9:c.196C>T
|
ENSP00000315774.5:p.Arg66Ter
|
|
ENST00000432321.6:n.313C>T
|
|
|
ENST00000453471.6:c.196C>T
|
ENSP00000403972.2:p.Arg66Ter
|
|
ENST00000525419.5:c.142C>T
|
ENSP00000433521.1:p.Arg48Ter
|
|
ENST00000525628.1:c.196C>T
|
ENSP00000432968.1:p.Arg66Ter
|
|
ENST00000526339.5:c.196C>T
|
ENSP00000436287.1:p.Arg66Ter
|
|
ENST00000526446.5:c.*251C>T
|
ENSP00000433645.1:n.*251C>T
|
|
ENST00000528492.1:c.-67+2276C>T
|
ENSP00000432848.1:n.-67+2276C>T
|
|
ENST00000529645.1:c.374C>T
|
ENSP00000431293.1:n.374C>T
|
|
ENST00000531228.1:c.*38C>T
|
ENSP00000433054.1:n.*38C>T
|
|
ENST00000532399.1:n.803C>T
|
|
|
NM_002496.3:c.196C>T
|
NP_002487.1:p.Arg66Ter
|
|
XM_005274013.1:c.196C>T
|
XP_005274070.1:p.Arg66Ter
|
|
XM_005274014.1:c.196C>T
|
XP_005274071.1:p.Arg66Ter
|
|
XM_005274015.1:c.76C>T
|
XP_005274072.1:p.Arg26Ter
|
|
XM_011545053.1:c.196C>T
|
XP_011543355.1:p.Arg66Ter
|
|
NM_002496.4:c.196C>T
MANE Select
|
NP_002487.1:p.Arg66Ter
|
|