ENST00000261024.7:c.217C>G
MANE Select
|
ENSP00000261024.3:p.Leu73Val
|
|
ENST00000261024.6:c.217C>G
|
ENSP00000261024.2:p.Leu73Val
|
|
ENST00000418714.1:n.658C>G
|
|
|
ENST00000427241.5:c.217C>G
|
ENSP00000390005.1:p.Leu73Val
|
|
ENST00000479598.5:n.498C>G
|
|
|
NM_014585.5:c.217C>G , LRG_837t1:c.217C>G
|
NP_055400.1:p.Leu73Val
|
|
XM_005246505.1:c.97C>G
|
XP_005246562.1:p.Leu33Val
|
|
XM_005246505.2:c.97C>G
|
XP_005246562.1:p.Leu33Val
|
|
XM_017003938.2:c.97C>G
|
XP_016859427.1:p.Leu33Val
|
|
NM_014585.6:c.217C>G
MANE Select
|
NP_055400.1:p.Leu73Val
|
|