ENST00000302850.10:c.3069C>G
MANE Select
|
ENSP00000303830.4:p.Ile1023Met
|
|
ENST00000302850.9:c.3069C>G
|
ENSP00000303830.4:p.Ile1023Met
|
|
ENST00000341500.9:c.3033C>G
|
ENSP00000342838.4:p.Ile1011Met
|
|
NM_000208.2:c.3069C>G
|
NP_000199.2:p.Ile1023Met
|
|
NM_000208.3:c.3069C>G
|
NP_000199.2:p.Ile1023Met
|
|
NM_001079817.1:c.3033C>G
|
NP_001073285.1:p.Ile1011Met
|
|
NM_001079817.2:c.3033C>G
|
NP_001073285.1:p.Ile1011Met
|
|
XM_011527988.1:c.3144C>G
|
XP_011526290.1:p.Ile1048Met
|
|
XM_011527989.1:c.3108C>G
|
XP_011526291.1:p.Ile1036Met
|
|
XM_011527988.2:c.3066C>G
|
XP_011526290.2:p.Ile1022Met
|
|
XM_011527989.3:c.3030C>G
|
XP_011526291.2:p.Ile1010Met
|
|
NM_000208.4:c.3069C>G
MANE Select
|
NP_000199.2:p.Ile1023Met
|
|
NM_001079817.3:c.3033C>G
|
NP_001073285.1:p.Ile1011Met
|
|