ENST00000553106.6:c.1102G>T
MANE Select
|
ENSP00000448059.1:p.Glu368Ter
|
|
ENST00000307000.7:c.1087G>T
|
ENSP00000303500.2:p.Glu363Ter
|
|
ENST00000549247.6:n.861G>T
|
|
|
ENST00000551114.2:n.764G>T
|
|
|
ENST00000553106.5:c.1102G>T
|
ENSP00000448059.1:p.Glu368Ter
|
|
ENST00000635477.1:c.206G>T
|
|
|
ENST00000635528.1:n.617G>T
|
|
|
NM_000277.1:c.1102G>T
|
NP_000268.1:p.Glu368Ter
|
|
XM_011538422.1:c.1045G>T
|
XP_011536724.1:p.Glu349Ter
|
|
NM_000277.2:c.1102G>T
|
NP_000268.1:p.Glu368Ter
|
|
NM_001354304.1:c.1102G>T
|
NP_001341233.1:p.Glu368Ter
|
|
NM_000277.3:c.1102G>T
MANE Select
|
NP_000268.1:p.Glu368Ter
|
|
NM_001354304.2:c.1102G>T
|
NP_001341233.1:p.Glu368Ter
|
|