ENST00000374479.4:c.1113C>G
MANE Select
|
ENSP00000363603.3:p.Ala371=
|
|
ENST00000374479.3:c.1113C>G
|
ENSP00000363603.3:p.Ala371=
|
|
NM_000147.4:c.1113C>G
|
NP_000138.2:p.Ala371=
|
|
XM_005245821.1:c.738C>G
|
XP_005245878.1:p.Ala246=
|
|
XM_011541167.1:c.480C>G
|
XP_011539469.1:p.Ala160=
|
|
XM_005245821.3:c.738C>G
|
XP_005245878.1:p.Ala246=
|
|
XM_011541167.3:c.480C>G
|
XP_011539469.1:p.Ala160=
|
|
XM_017000905.2:c.810C>G
|
XP_016856394.1:p.Ala270=
|
|
NM_000147.5:c.1113C>G
MANE Select
|
NP_000138.2:p.Ala371=
|
|
NR_174379.1:n.1291C>G
|
|
|
NR_174380.1:n.1340C>G
|
|
|
NR_174381.1:n.1179C>G
|
|
|
NR_174382.1:n.1576C>G
|
|
|