ENST00000302850.10:c.3905C>G
MANE Select
|
ENSP00000303830.4:p.Ser1302Trp
|
|
ENST00000302850.9:c.3905C>G
|
ENSP00000303830.4:p.Ser1302Trp
|
|
ENST00000341500.9:c.3869C>G
|
ENSP00000342838.4:p.Ser1290Trp
|
|
NM_000208.2:c.3905C>G
|
NP_000199.2:p.Ser1302Trp
|
|
NM_000208.3:c.3905C>G
|
NP_000199.2:p.Ser1302Trp
|
|
NM_001079817.1:c.3869C>G
|
NP_001073285.1:p.Ser1290Trp
|
|
NM_001079817.2:c.3869C>G
|
NP_001073285.1:p.Ser1290Trp
|
|
XM_011527988.1:c.3980C>G
|
XP_011526290.1:p.Ser1327Trp
|
|
XM_011527989.1:c.3944C>G
|
XP_011526291.1:p.Ser1315Trp
|
|
XM_011527988.2:c.3902C>G
|
XP_011526290.2:p.Ser1301Trp
|
|
XM_011527989.3:c.3866C>G
|
XP_011526291.2:p.Ser1289Trp
|
|
NM_000208.4:c.3905C>G
MANE Select
|
NP_000199.2:p.Ser1302Trp
|
|
NM_001079817.3:c.3869C>G
|
NP_001073285.1:p.Ser1290Trp
|
|