ENST00000302850.10:c.2389C>G
MANE Select
|
ENSP00000303830.4:p.Pro797Ala
|
|
ENST00000302850.9:c.2389C>G
|
ENSP00000303830.4:p.Pro797Ala
|
|
ENST00000341500.9:c.2353C>G
|
ENSP00000342838.4:p.Pro785Ala
|
|
ENST00000597211.1:n.72C>G
|
|
|
NM_000208.2:c.2389C>G
|
NP_000199.2:p.Pro797Ala
|
|
NM_000208.3:c.2389C>G
|
NP_000199.2:p.Pro797Ala
|
|
NM_001079817.1:c.2353C>G
|
NP_001073285.1:p.Pro785Ala
|
|
NM_001079817.2:c.2353C>G
|
NP_001073285.1:p.Pro785Ala
|
|
XM_011527988.1:c.2467C>G
|
XP_011526290.1:p.Pro823Ala
|
|
XM_011527989.1:c.2431C>G
|
XP_011526291.1:p.Pro811Ala
|
|
XM_011527988.2:c.2389C>G
|
XP_011526290.2:p.Pro797Ala
|
|
XM_011527989.3:c.2353C>G
|
XP_011526291.2:p.Pro785Ala
|
|
NM_000208.4:c.2389C>G
MANE Select
|
NP_000199.2:p.Pro797Ala
|
|
NM_001079817.3:c.2353C>G
|
NP_001073285.1:p.Pro785Ala
|
|