ENST00000374479.4:c.1085T>G
MANE Select
|
ENSP00000363603.3:p.Leu362Arg
|
|
ENST00000374479.3:c.1085T>G
|
ENSP00000363603.3:p.Leu362Arg
|
|
NM_000147.4:c.1085T>G
|
NP_000138.2:p.Leu362Arg
|
|
XM_005245821.1:c.710T>G
|
XP_005245878.1:p.Leu237Arg
|
|
XM_011541167.1:c.452T>G
|
XP_011539469.1:p.Leu151Arg
|
|
XM_005245821.3:c.710T>G
|
XP_005245878.1:p.Leu237Arg
|
|
XM_011541167.3:c.452T>G
|
XP_011539469.1:p.Leu151Arg
|
|
XM_017000905.2:c.782T>G
|
XP_016856394.1:p.Leu261Arg
|
|
NM_000147.5:c.1085T>G
MANE Select
|
NP_000138.2:p.Leu362Arg
|
|
NR_174379.1:n.1263T>G
|
|
|
NR_174380.1:n.1312T>G
|
|
|
NR_174381.1:n.1151T>G
|
|
|
NR_174382.1:n.1548T>G
|
|
|