ENST00000302850.10:c.3595C>G
MANE Select
|
ENSP00000303830.4:p.Pro1199Ala
|
|
ENST00000302850.9:c.3595C>G
|
ENSP00000303830.4:p.Pro1199Ala
|
|
ENST00000341500.9:c.3559C>G
|
ENSP00000342838.4:p.Pro1187Ala
|
|
ENST00000601099.1:n.506C>G
|
|
|
NM_000208.2:c.3595C>G
|
NP_000199.2:p.Pro1199Ala
|
|
NM_000208.3:c.3595C>G
|
NP_000199.2:p.Pro1199Ala
|
|
NM_001079817.1:c.3559C>G
|
NP_001073285.1:p.Pro1187Ala
|
|
NM_001079817.2:c.3559C>G
|
NP_001073285.1:p.Pro1187Ala
|
|
XM_011527988.1:c.3670C>G
|
XP_011526290.1:p.Pro1224Ala
|
|
XM_011527989.1:c.3634C>G
|
XP_011526291.1:p.Pro1212Ala
|
|
XM_011527988.2:c.3592C>G
|
XP_011526290.2:p.Pro1198Ala
|
|
XM_011527989.3:c.3556C>G
|
XP_011526291.2:p.Pro1186Ala
|
|
NM_000208.4:c.3595C>G
MANE Select
|
NP_000199.2:p.Pro1199Ala
|
|
NM_001079817.3:c.3559C>G
|
NP_001073285.1:p.Pro1187Ala
|
|