ENST00000248633.9:c.2300T>G
MANE Select
|
ENSP00000248633.4:p.Leu767Arg
|
|
ENST00000248633.8:c.2300T>G
|
ENSP00000248633.4:p.Leu767Arg
|
|
ENST00000428214.5:c.2129T>G
|
ENSP00000394413.1:p.Leu710Arg
|
|
ENST00000438045.5:c.1334T>G
|
ENSP00000410438.1:p.Leu445Arg
|
|
ENST00000484913.5:n.2339T>G
|
|
|
ENST00000496092.1:n.98T>G
|
|
|
ENST00000496420.5:n.1976T>G
|
|
|
NM_000466.2:c.2300T>G
|
NP_000457.1:p.Leu767Arg
|
|
NM_001282677.1:c.2129T>G
|
NP_001269606.1:p.Leu710Arg
|
|
NM_001282678.1:c.1676T>G
|
NP_001269607.1:p.Leu559Arg
|
|
XM_005250433.3:c.551T>G
|
XP_005250490.1:p.Leu184Arg
|
|
XR_242246.3:n.2396T>G
|
|
|
XM_017012319.2:c.551T>G
|
XP_016867808.1:p.Leu184Arg
|
|
XR_001744808.2:n.1327T>G
|
|
|
XR_242246.5:n.2347T>G
|
|
|
NM_000466.3:c.2300T>G
MANE Select
|
NP_000457.1:p.Leu767Arg
|
|
NM_001282677.2:c.2129T>G
|
NP_001269606.1:p.Leu710Arg
|
|
NM_001282678.2:c.1676T>G
|
NP_001269607.1:p.Leu559Arg
|
|