ENST00000302850.10:c.3895C>A
MANE Select
|
ENSP00000303830.4:p.Pro1299Thr
|
|
ENST00000302850.9:c.3895C>A
|
ENSP00000303830.4:p.Pro1299Thr
|
|
ENST00000341500.9:c.3859C>A
|
ENSP00000342838.4:p.Pro1287Thr
|
|
NM_000208.2:c.3895C>A
|
NP_000199.2:p.Pro1299Thr
|
|
NM_000208.3:c.3895C>A
|
NP_000199.2:p.Pro1299Thr
|
|
NM_001079817.1:c.3859C>A
|
NP_001073285.1:p.Pro1287Thr
|
|
NM_001079817.2:c.3859C>A
|
NP_001073285.1:p.Pro1287Thr
|
|
XM_011527988.1:c.3970C>A
|
XP_011526290.1:p.Pro1324Thr
|
|
XM_011527989.1:c.3934C>A
|
XP_011526291.1:p.Pro1312Thr
|
|
XM_011527988.2:c.3892C>A
|
XP_011526290.2:p.Pro1298Thr
|
|
XM_011527989.3:c.3856C>A
|
XP_011526291.2:p.Pro1286Thr
|
|
NM_000208.4:c.3895C>A
MANE Select
|
NP_000199.2:p.Pro1299Thr
|
|
NM_001079817.3:c.3859C>A
|
NP_001073285.1:p.Pro1287Thr
|
|