ENST00000376059.8:c.194T>G
MANE Select
|
ENSP00000365227.3:p.Ile65Ser
|
|
ENST00000337917.11:c.236T>G
|
ENSP00000338776.7:p.Ile79Ser
|
|
ENST00000376049.4:c.32T>G
|
ENSP00000365217.4:p.Ile11Ser
|
|
ENST00000376059.7:c.194T>G
|
ENSP00000365227.3:p.Ile65Ser
|
|
ENST00000466820.1:n.611T>G
|
|
|
ENST00000497362.5:n.613T>G
|
|
|
NM_001623.3:c.194T>G
|
NP_001614.3:p.Ile65Ser
|
|
NM_004847.3:c.32T>G
|
NP_004838.1:p.Ile11Ser
|
|
NM_032955.1:c.32T>G
|
NP_116573.1:p.Ile11Ser
|
|
XM_005248870.3:c.194T>G
|
XP_005248927.1:p.Ile65Ser
|
|
XM_005248871.1:c.257T>G
|
XP_005248928.1:p.Ile86Ser
|
|
NM_001318970.1:c.32T>G
|
NP_001305899.1:p.Ile11Ser
|
|
NM_001623.4:c.194T>G
|
NP_001614.3:p.Ile65Ser
|
|
NM_032955.2:c.32T>G
|
NP_116573.1:p.Ile11Ser
|
|
XM_005248870.4:c.194T>G
|
XP_005248927.1:p.Ile65Ser
|
|
XM_017010332.1:c.32T>G
|
XP_016865821.1:p.Ile11Ser
|
|
NM_001623.5:c.194T>G
MANE Select
|
NP_001614.3:p.Ile65Ser
|
|
NM_001318970.2:c.32T>G
|
NP_001305899.1:p.Ile11Ser
|
|
NM_032955.3:c.32T>G
|
NP_116573.1:p.Ile11Ser
|
|