ENST00000302850.10:c.4135T>A
MANE Select
|
ENSP00000303830.4:p.Ser1379Thr
|
|
ENST00000302850.9:c.4135T>A
|
ENSP00000303830.4:p.Ser1379Thr
|
|
ENST00000341500.9:c.4099T>A
|
ENSP00000342838.4:p.Ser1367Thr
|
|
NM_000208.2:c.4135T>A
|
NP_000199.2:p.Ser1379Thr
|
|
NM_000208.3:c.4135T>A
|
NP_000199.2:p.Ser1379Thr
|
|
NM_001079817.1:c.4099T>A
|
NP_001073285.1:p.Ser1367Thr
|
|
NM_001079817.2:c.4099T>A
|
NP_001073285.1:p.Ser1367Thr
|
|
XM_011527988.1:c.4210T>A
|
XP_011526290.1:p.Ser1404Thr
|
|
XM_011527989.1:c.4174T>A
|
XP_011526291.1:p.Ser1392Thr
|
|
XM_011527988.2:c.4132T>A
|
XP_011526290.2:p.Ser1378Thr
|
|
XM_011527989.3:c.4096T>A
|
XP_011526291.2:p.Ser1366Thr
|
|
NM_000208.4:c.4135T>A
MANE Select
|
NP_000199.2:p.Ser1379Thr
|
|
NM_001079817.3:c.4099T>A
|
NP_001073285.1:p.Ser1367Thr
|
|