ENST00000642683.1:c.733C>G
|
ENSP00000495376.1:p.Leu245Val
|
|
ENST00000643672.1:c.730C>G
|
ENSP00000494532.1:p.Leu244Val
|
|
ENST00000645280.1:c.727C>G
|
ENSP00000496690.1:p.Leu243Val
|
|
ENST00000648579.1:c.*78C>G
|
ENSP00000497638.1:n.*78C>G
|
|
ENST00000650617.1:c.781C>G
MANE Select
|
ENSP00000497532.1:p.Leu261Val
|
|
ENST00000273158.8:c.781C>G
|
ENSP00000273158.3:p.Leu261Val
|
|
NM_017875.2:c.781C>G
|
NP_060345.2:p.Leu261Val
|
|
XM_006713214.1:c.769C>G
|
XP_006713277.1:p.Leu257Val
|
|
XM_011533869.1:c.763C>G
|
XP_011532171.1:p.Leu255Val
|
|
XM_011533870.1:c.730C>G
|
XP_011532172.1:p.Leu244Val
|
|
XM_011533871.1:c.601C>G
|
XP_011532173.1:p.Leu201Val
|
|
NM_001354798.1:c.626-1833C>G
|
NP_001341727.1:n.626-1833C>G
|
|
NM_017875.4:c.781C>G
MANE Select
|
NP_060345.2:p.Leu261Val
|
|
XM_006713214.2:c.769C>G
|
XP_006713277.1:p.Leu257Val
|
|
XM_011533869.2:c.763C>G
|
XP_011532171.1:p.Leu255Val
|
|
XM_024453611.1:c.727C>G
|
XP_024309379.1:p.Leu243Val
|
|
NM_001354798.2:c.626-1833C>G
|
NP_001341727.1:n.626-1833C>G
|
|