|
NM_001985.3:c.253C>T
MANE Select
|
NP_001976.1:p.Arg85Ter
|
|
ENST00000309244.9:c.253C>T
MANE Select
|
ENSP00000311930.3:p.Arg85Ter
|
|
NM_001014763.1:c.526C>T
|
NP_001014763.1:p.Arg176Ter
|
|
NM_001985.2:c.253C>T
|
NP_001976.1:p.Arg85Ter
|
|
ENST00000309244.8:c.253C>T
|
ENSP00000311930.3:p.Arg85Ter
|
|
ENST00000354232.8:c.526C>T
|
ENSP00000346173.3:p.Arg176Ter
|
|
ENST00000593992.1:n.276C>T
|
|
|
ENST00000596253.1:c.216+896C>T
|
ENSP00000469628.1:n.216+896C>T
|
|
ENST00000600067.1:c.*179C>T
|
ENSP00000469452.1:n.*179C>T
|
|
XM_024451418.1:c.142C>T
|
XP_024307186.1:p.Arg48Ter
|