ENST00000302850.10:c.3597T=
MANE Select
|
ENSP00000303830.4:p.Pro1199=
|
|
ENST00000302850.9:c.3597T=
|
ENSP00000303830.4:p.Pro1199=
|
|
ENST00000341500.9:c.3561T=
|
ENSP00000342838.4:p.Pro1187=
|
|
ENST00000601099.1:n.508T=
|
|
|
NM_000208.2:c.3597T=
|
NP_000199.2:p.Pro1199=
|
|
NM_000208.3:c.3597T=
|
NP_000199.2:p.Pro1199=
|
|
NM_001079817.1:c.3561T=
|
NP_001073285.1:p.Pro1187=
|
|
NM_001079817.2:c.3561T=
|
NP_001073285.1:p.Pro1187=
|
|
XM_011527988.1:c.3672T=
|
XP_011526290.1:p.Pro1224=
|
|
XM_011527989.1:c.3636T=
|
XP_011526291.1:p.Pro1212=
|
|
XM_011527988.2:c.3594T=
|
XP_011526290.2:p.Pro1198=
|
|
XM_011527989.3:c.3558T=
|
XP_011526291.2:p.Pro1186=
|
|
NM_000208.4:c.3597T=
MANE Select
|
NP_000199.2:p.Pro1199=
|
|
NM_001079817.3:c.3561T=
|
NP_001073285.1:p.Pro1187=
|
|