ENST00000268125.10:c.642T>A
MANE Select
|
ENSP00000268125.5:p.Ser214Arg
|
|
ENST00000268125.9:c.642T>A
|
ENSP00000268125.5:p.Ser214Arg
|
|
ENST00000563254.1:c.59T>A
|
|
|
ENST00000567787.1:c.*220T>A
|
ENSP00000457251.1:n.*220T>A
|
|
NM_000326.4:c.642T>A
|
NP_000317.1:p.Ser214Arg
|
|
XM_011521870.1:c.642T>A
|
XP_011520172.1:p.Ser214Arg
|
|
XM_011521871.1:c.567T>A
|
XP_011520173.1:p.Ser189Arg
|
|
XM_011521872.1:c.567T>A
|
XP_011520174.1:p.Ser189Arg
|
|
XM_011521870.2:c.642T>A
|
XP_011520172.1:p.Ser214Arg
|
|
XM_017022460.1:c.669T>A
|
XP_016877949.1:p.Ser223Arg
|
|
NM_000326.5:c.642T>A
MANE Select
|
NP_000317.1:p.Ser214Arg
|
|