ENST00000553106.6:c.1105C>T
MANE Select
|
ENSP00000448059.1:p.Leu369=
|
|
ENST00000307000.7:c.1090C>T
|
ENSP00000303500.2:p.Leu364=
|
|
ENST00000549247.6:n.864C>T
|
|
|
ENST00000551114.2:n.767C>T
|
|
|
ENST00000553106.5:c.1105C>T
|
ENSP00000448059.1:p.Leu369=
|
|
ENST00000635477.1:c.209C>T
|
|
|
ENST00000635528.1:n.620C>T
|
|
|
NM_000277.1:c.1105C>T
|
NP_000268.1:p.Leu369=
|
|
XM_011538422.1:c.1048C>T
|
XP_011536724.1:p.Leu350=
|
|
NM_000277.2:c.1105C>T
|
NP_000268.1:p.Leu369=
|
|
NM_001354304.1:c.1105C>T
|
NP_001341233.1:p.Leu369=
|
|
NM_000277.3:c.1105C>T
MANE Select
|
NP_000268.1:p.Leu369=
|
|
NM_001354304.2:c.1105C>T
|
NP_001341233.1:p.Leu369=
|
|