ENST00000553106.6:c.1103A>T
MANE Select
|
ENSP00000448059.1:p.Glu368Val
|
|
ENST00000307000.7:c.1088A>T
|
ENSP00000303500.2:p.Glu363Val
|
|
ENST00000549247.6:n.862A>T
|
|
|
ENST00000551114.2:n.765A>T
|
|
|
ENST00000553106.5:c.1103A>T
|
ENSP00000448059.1:p.Glu368Val
|
|
ENST00000635477.1:c.207A>T
|
|
|
ENST00000635528.1:n.618A>T
|
|
|
NM_000277.1:c.1103A>T
|
NP_000268.1:p.Glu368Val
|
|
XM_011538422.1:c.1046A>T
|
XP_011536724.1:p.Glu349Val
|
|
NM_000277.2:c.1103A>T
|
NP_000268.1:p.Glu368Val
|
|
NM_001354304.1:c.1103A>T
|
NP_001341233.1:p.Glu368Val
|
|
NM_000277.3:c.1103A>T
MANE Select
|
NP_000268.1:p.Glu368Val
|
|
NM_001354304.2:c.1103A>T
|
NP_001341233.1:p.Glu368Val
|
|