ENST00000302850.10:c.3886C>A
MANE Select
|
ENSP00000303830.4:p.Pro1296Thr
|
|
ENST00000302850.9:c.3886C>A
|
ENSP00000303830.4:p.Pro1296Thr
|
|
ENST00000341500.9:c.3850C>A
|
ENSP00000342838.4:p.Pro1284Thr
|
|
NM_000208.2:c.3886C>A
|
NP_000199.2:p.Pro1296Thr
|
|
NM_000208.3:c.3886C>A
|
NP_000199.2:p.Pro1296Thr
|
|
NM_001079817.1:c.3850C>A
|
NP_001073285.1:p.Pro1284Thr
|
|
NM_001079817.2:c.3850C>A
|
NP_001073285.1:p.Pro1284Thr
|
|
XM_011527988.1:c.3961C>A
|
XP_011526290.1:p.Pro1321Thr
|
|
XM_011527989.1:c.3925C>A
|
XP_011526291.1:p.Pro1309Thr
|
|
XM_011527988.2:c.3883C>A
|
XP_011526290.2:p.Pro1295Thr
|
|
XM_011527989.3:c.3847C>A
|
XP_011526291.2:p.Pro1283Thr
|
|
NM_000208.4:c.3886C>A
MANE Select
|
NP_000199.2:p.Pro1296Thr
|
|
NM_001079817.3:c.3850C>A
|
NP_001073285.1:p.Pro1284Thr
|
|