|
NM_002892.4:c.2614G>T
MANE Select
|
NP_002883.3:p.Glu872Ter
|
|
ENST00000355431.8:c.2614G>T
MANE Select
|
ENSP00000347602.3:p.Glu872Ter
|
|
NM_002892.3:c.2614G>T
|
NP_002883.3:p.Glu872Ter
|
|
NM_023000.2:c.2614G>T
|
NP_075376.2:p.Glu872Ter
|
|
NM_023000.3:c.2614G>T
|
NP_075376.2:p.Glu872Ter
|
|
NM_023001.2:c.2614G>T
|
NP_075377.2:p.Glu872Ter
|
|
NM_023001.3:c.2614G>T
|
NP_075377.2:p.Glu872Ter
|
|
ENST00000348476.7:c.2614G>T
|
ENSP00000344556.3:p.Glu872Ter
|
|
ENST00000355431.7:c.2614G>T
|
ENSP00000347602.3:p.Glu872Ter
|
|
ENST00000395168.7:c.2614G>T
|
ENSP00000378597.3:p.Glu872Ter
|
|
ENST00000417477.2:c.1648G>T
|
ENSP00000416053.2:p.Glu550Ter
|
|
ENST00000431317.6:c.2614G>T
|
ENSP00000397368.2:p.Glu872Ter
|
|
XM_005267964.1:c.2674G>T
|
XP_005268021.1:p.Glu892Ter
|
|
XM_005267964.2:c.2674G>T
|
XP_005268021.1:p.Glu892Ter
|
|
XM_005267965.1:c.2674G>T
|
XP_005268022.1:p.Glu892Ter
|
|
XM_005267965.2:c.2674G>T
|
XP_005268022.1:p.Glu892Ter
|
|
XM_011537054.1:c.2674G>T
|
XP_011535356.1:p.Glu892Ter
|
|
XM_011537055.1:c.2401G>T
|
XP_011535357.1:p.Glu801Ter
|
|
XM_011537056.1:c.1708G>T
|
XP_011535358.1:p.Glu570Ter
|
|
XM_017021560.1:c.2674G>T
|
XP_016877049.1:p.Glu892Ter
|
|
XM_017021561.1:c.2674G>T
|
XP_016877050.1:p.Glu892Ter
|
|
XM_017021562.1:c.2614G>T
|
XP_016877051.1:p.Glu872Ter
|
|
XM_017021563.1:c.2674G>T
|
XP_016877052.1:p.Glu892Ter
|
|
XM_017021564.1:c.2233G>T
|
XP_016877053.1:p.Glu745Ter
|
|
XM_017021565.1:c.1648G>T
|
XP_016877054.1:p.Glu550Ter
|
|
XM_024449683.1:c.967G>T
|
XP_024305451.1:p.Glu323Ter
|
|
XM_024449684.1:c.907G>T
|
XP_024305452.1:p.Glu303Ter
|