ENST00000302850.10:c.3590T>G
MANE Select
|
ENSP00000303830.4:p.Leu1197Arg
|
|
ENST00000302850.9:c.3590T>G
|
ENSP00000303830.4:p.Leu1197Arg
|
|
ENST00000341500.9:c.3554T>G
|
ENSP00000342838.4:p.Leu1185Arg
|
|
ENST00000601099.1:n.501T>G
|
|
|
NM_000208.2:c.3590T>G
|
NP_000199.2:p.Leu1197Arg
|
|
NM_000208.3:c.3590T>G
|
NP_000199.2:p.Leu1197Arg
|
|
NM_001079817.1:c.3554T>G
|
NP_001073285.1:p.Leu1185Arg
|
|
NM_001079817.2:c.3554T>G
|
NP_001073285.1:p.Leu1185Arg
|
|
XM_011527988.1:c.3665T>G
|
XP_011526290.1:p.Leu1222Arg
|
|
XM_011527989.1:c.3629T>G
|
XP_011526291.1:p.Leu1210Arg
|
|
XM_011527988.2:c.3587T>G
|
XP_011526290.2:p.Leu1196Arg
|
|
XM_011527989.3:c.3551T>G
|
XP_011526291.2:p.Leu1184Arg
|
|
NM_000208.4:c.3590T>G
MANE Select
|
NP_000199.2:p.Leu1197Arg
|
|
NM_001079817.3:c.3554T>G
|
NP_001073285.1:p.Leu1185Arg
|
|