ENST00000284885.8:c.2611C>T
MANE Select
|
ENSP00000284885.3:p.Arg871Ter
|
|
ENST00000284885.7:c.2611C>T
|
ENSP00000284885.3:p.Arg871Ter
|
|
NM_002772.2:c.2611C>T
|
NP_002763.2:p.Arg871Ter
|
|
XM_011529654.1:c.2746C>T
|
XP_011527956.1:p.Arg916Ter
|
|
XM_011529655.1:c.2746C>T
|
XP_011527957.1:p.Arg916Ter
|
|
XM_011529656.1:c.2746C>T
|
XP_011527958.1:p.Arg916Ter
|
|
XM_011529657.1:c.2701C>T
|
XP_011527959.1:p.Arg901Ter
|
|
XM_011529658.1:c.2665C>T
|
XP_011527960.1:p.Arg889Ter
|
|
XM_011529659.1:c.2656C>T
|
XP_011527961.1:p.Arg886Ter
|
|
XM_011529654.2:c.2746C>T
|
XP_011527956.1:p.Arg916Ter
|
|
XM_011529656.2:c.2746C>T
|
XP_011527958.1:p.Arg916Ter
|
|
XM_011529657.2:c.2701C>T
|
XP_011527959.1:p.Arg901Ter
|
|
XM_011529658.2:c.2665C>T
|
XP_011527960.1:p.Arg889Ter
|
|
NM_002772.3:c.2611C>T
MANE Select
|
NP_002763.3:p.Arg871Ter
|
|