ENST00000497571.6:c.477T>G
MANE Select
|
ENSP00000419923.1:p.Ser159=
|
|
ENST00000173785.4:n.212T>G
|
|
|
ENST00000380946.3:n.712T>G
|
|
|
ENST00000469435.1:c.477T>G
|
ENSP00000419079.1:p.Ser159=
|
|
ENST00000497571.5:c.477T>G
|
ENSP00000419923.1:p.Ser159=
|
|
ENST00000542957.1:c.477T>G
|
ENSP00000445301.1:p.Ser159=
|
|
NM_001160124.1:c.477T>G
|
NP_001153596.1:p.Ser159=
|
|
NM_001160125.1:c.477T>G
|
NP_001153597.1:p.Ser159=
|
|
NM_001300.5:c.477T>G
|
NP_001291.3:p.Ser159=
|
|
NR_027653.1:n.744T>G
|
|
|
NM_001300.6:c.477T>G
MANE Select
|
NP_001291.3:p.Ser159=
|
|
NM_001160124.2:c.477T>G
|
NP_001153596.1:p.Ser159=
|
|
NR_027653.2:n.672T>G
|
|
|
NM_001160125.2:c.477T>G
|
NP_001153597.1:p.Ser159=
|
|