|
ENST00000553106.6:c.151G=
MANE Select
|
ENSP00000448059.1:p.Val51=
|
|
|
ENST00000307000.7:c.136G=
|
ENSP00000303500.2:p.Val46=
|
|
|
ENST00000546844.1:c.151G=
|
ENSP00000446658.1:p.Val51=
|
|
|
ENST00000548677.2:n.238G=
|
|
|
|
ENST00000548928.1:n.73G=
|
|
|
|
ENST00000549111.5:n.247G=
|
|
|
|
ENST00000550978.6:c.135G=
|
|
|
|
ENST00000551337.5:c.151G=
|
ENSP00000447620.1:p.Val51=
|
|
|
ENST00000551988.5:n.240G=
|
|
|
|
ENST00000553106.5:c.151G=
|
ENSP00000448059.1:p.Val51=
|
|
|
ENST00000635500.1:n.119G=
|
|
|
|
NM_000277.1:c.151G=
|
NP_000268.1:p.Val51=
|
|
|
XM_011538422.1:c.151G=
|
XP_011536724.1:p.Val51=
|
|
|
NM_000277.2:c.151G=
|
NP_000268.1:p.Val51=
|
|
|
NM_001354304.1:c.151G=
|
NP_001341233.1:p.Val51=
|
|
|
XM_017019370.2:c.151G=
|
XP_016874859.1:p.Val51=
|
|
|
NM_000277.3:c.151G=
MANE Select
|
NP_000268.1:p.Val51=
|
|
|
NM_001354304.2:c.151G=
|
NP_001341233.1:p.Val51=
|
|
