ENST00000302850.10:c.2869A>G
MANE Select
|
ENSP00000303830.4:p.Ile957Val
|
|
ENST00000302850.9:c.2869A>G
|
ENSP00000303830.4:p.Ile957Val
|
|
ENST00000341500.9:c.2833A>G
|
ENSP00000342838.4:p.Ile945Val
|
|
NM_000208.2:c.2869A>G
|
NP_000199.2:p.Ile957Val
|
|
NM_000208.3:c.2869A>G
|
NP_000199.2:p.Ile957Val
|
|
NM_001079817.1:c.2833A>G
|
NP_001073285.1:p.Ile945Val
|
|
NM_001079817.2:c.2833A>G
|
NP_001073285.1:p.Ile945Val
|
|
XM_011527988.1:c.2944A>G
|
XP_011526290.1:p.Ile982Val
|
|
XM_011527989.1:c.2908A>G
|
XP_011526291.1:p.Ile970Val
|
|
XM_011527988.2:c.2866A>G
|
XP_011526290.2:p.Ile956Val
|
|
XM_011527989.3:c.2830A>G
|
XP_011526291.2:p.Ile944Val
|
|
NM_000208.4:c.2869A>G
MANE Select
|
NP_000199.2:p.Ile957Val
|
|
NM_001079817.3:c.2833A>G
|
NP_001073285.1:p.Ile945Val
|
|