ENST00000553106.6:c.433G>C
MANE Select
|
ENSP00000448059.1:p.Asp145His
|
|
ENST00000307000.7:c.418G>C
|
ENSP00000303500.2:p.Asp140His
|
|
ENST00000549111.5:n.529G>C
|
|
|
ENST00000550978.6:c.417G>C
|
|
|
ENST00000551988.5:n.522G>C
|
|
|
ENST00000553106.5:c.433G>C
|
ENSP00000448059.1:p.Asp145His
|
|
NM_000277.1:c.433G>C
|
NP_000268.1:p.Asp145His
|
|
XM_011538422.1:c.433G>C
|
XP_011536724.1:p.Asp145His
|
|
NM_000277.2:c.433G>C
|
NP_000268.1:p.Asp145His
|
|
NM_001354304.1:c.433G>C
|
NP_001341233.1:p.Asp145His
|
|
XM_017019370.2:c.433G>C
|
XP_016874859.1:p.Asp145His
|
|
NM_000277.3:c.433G>C
MANE Select
|
NP_000268.1:p.Asp145His
|
|
NM_001354304.2:c.433G>C
|
NP_001341233.1:p.Asp145His
|
|