ENST00000374479.4:c.1090A>G
MANE Select
|
ENSP00000363603.3:p.Ile364Val
|
|
ENST00000374479.3:c.1090A>G
|
ENSP00000363603.3:p.Ile364Val
|
|
NM_000147.4:c.1090A>G
|
NP_000138.2:p.Ile364Val
|
|
XM_005245821.1:c.715A>G
|
XP_005245878.1:p.Ile239Val
|
|
XM_011541167.1:c.457A>G
|
XP_011539469.1:p.Ile153Val
|
|
XM_005245821.3:c.715A>G
|
XP_005245878.1:p.Ile239Val
|
|
XM_011541167.3:c.457A>G
|
XP_011539469.1:p.Ile153Val
|
|
XM_017000905.2:c.787A>G
|
XP_016856394.1:p.Ile263Val
|
|
NM_000147.5:c.1090A>G
MANE Select
|
NP_000138.2:p.Ile364Val
|
|
NR_174379.1:n.1268A>G
|
|
|
NR_174380.1:n.1317A>G
|
|
|
NR_174381.1:n.1156A>G
|
|
|
NR_174382.1:n.1553A>G
|
|
|