ENST00000302850.10:c.3886C>T
MANE Select
|
ENSP00000303830.4:p.Pro1296Ser
|
|
ENST00000302850.9:c.3886C>T
|
ENSP00000303830.4:p.Pro1296Ser
|
|
ENST00000341500.9:c.3850C>T
|
ENSP00000342838.4:p.Pro1284Ser
|
|
NM_000208.2:c.3886C>T
|
NP_000199.2:p.Pro1296Ser
|
|
NM_000208.3:c.3886C>T
|
NP_000199.2:p.Pro1296Ser
|
|
NM_001079817.1:c.3850C>T
|
NP_001073285.1:p.Pro1284Ser
|
|
NM_001079817.2:c.3850C>T
|
NP_001073285.1:p.Pro1284Ser
|
|
XM_011527988.1:c.3961C>T
|
XP_011526290.1:p.Pro1321Ser
|
|
XM_011527989.1:c.3925C>T
|
XP_011526291.1:p.Pro1309Ser
|
|
XM_011527988.2:c.3883C>T
|
XP_011526290.2:p.Pro1295Ser
|
|
XM_011527989.3:c.3847C>T
|
XP_011526291.2:p.Pro1283Ser
|
|
NM_000208.4:c.3886C>T
MANE Select
|
NP_000199.2:p.Pro1296Ser
|
|
NM_001079817.3:c.3850C>T
|
NP_001073285.1:p.Pro1284Ser
|
|