NM_004750.5:c.356G>A
MANE Select
|
NP_004741.1:p.Arg119His
|
ENST00000392386.8:c.356G>A
MANE Select
|
ENSP00000376188.2:p.Arg119His
|
NM_004750.4:c.356G>A
|
NP_004741.1:p.Arg119His
|
ENST00000392386.7:c.356G>A
|
ENSP00000376188.2:p.Arg119His
|
ENST00000684169.1:c.356G>A
|
ENSP00000506849.1:p.Arg119His
|
XM_011528422.1:c.290G>A
|
XP_011526724.1:p.Arg97His
|
XM_011528422.2:c.290G>A
|
XP_011526724.1:p.Arg97His
|
XM_011528423.1:c.356G>A
|
XP_011526725.1:p.Arg119His
|
XM_011528423.2:c.356G>A
|
XP_011526725.1:p.Arg119His
|
XM_011528424.1:c.290G>A
|
XP_011526726.1:p.Arg97His
|
XM_011528424.3:c.290G>A
|
XP_011526726.1:p.Arg97His
|