ENST00000553106.6:c.123C>G
MANE Select
|
ENSP00000448059.1:p.Leu41=
|
|
ENST00000307000.7:c.108C>G
|
ENSP00000303500.2:p.Leu36=
|
|
ENST00000546844.1:c.123C>G
|
ENSP00000446658.1:p.Leu41=
|
|
ENST00000548677.2:n.210C>G
|
|
|
ENST00000548928.1:n.45C>G
|
|
|
ENST00000549111.5:n.219C>G
|
|
|
ENST00000550978.6:c.107C>G
|
|
|
ENST00000551337.5:c.123C>G
|
ENSP00000447620.1:p.Leu41=
|
|
ENST00000551988.5:n.212C>G
|
|
|
ENST00000553106.5:c.123C>G
|
ENSP00000448059.1:p.Leu41=
|
|
ENST00000635500.1:n.91C>G
|
|
|
NM_000277.1:c.123C>G
|
NP_000268.1:p.Leu41=
|
|
XM_011538422.1:c.123C>G
|
XP_011536724.1:p.Leu41=
|
|
NM_000277.2:c.123C>G
|
NP_000268.1:p.Leu41=
|
|
NM_001354304.1:c.123C>G
|
NP_001341233.1:p.Leu41=
|
|
XM_017019370.2:c.123C>G
|
XP_016874859.1:p.Leu41=
|
|
NM_000277.3:c.123C>G
MANE Select
|
NP_000268.1:p.Leu41=
|
|
NM_001354304.2:c.123C>G
|
NP_001341233.1:p.Leu41=
|
|