ENST00000314251.8:c.581T>G
MANE Select
|
ENSP00000323568.3:p.Leu194Arg
|
|
ENST00000314251.7:c.581T>G
|
ENSP00000323568.3:p.Leu194Arg
|
|
ENST00000461867.1:c.62T>G
|
ENSP00000418888.1:p.Leu21Arg
|
|
ENST00000469787.1:c.*48T>G
|
ENSP00000417918.1:n.*48T>G
|
|
ENST00000471379.1:n.292T>G
|
|
|
ENST00000497642.5:c.*48T>G
|
ENSP00000418456.1:n.*48T>G
|
|
NM_000340.1:c.581T>G
|
NP_000331.1:p.Leu194Arg
|
|
NM_001278658.1:c.224T>G
|
NP_001265587.1:p.Leu75Arg
|
|
NM_001278659.1:c.62T>G
|
NP_001265588.1:p.Leu21Arg
|
|
XM_011513087.1:c.536T>G
|
XP_011511389.1:p.Leu179Arg
|
|
XM_011513088.1:c.362T>G
|
XP_011511390.1:p.Leu121Arg
|
|
XM_011513089.1:c.62T>G
|
XP_011511391.1:p.Leu21Arg
|
|
XM_011513087.2:c.536T>G
|
XP_011511389.1:p.Leu179Arg
|
|
XM_024453720.1:c.62T>G
|
XP_024309488.1:p.Leu21Arg
|
|
NM_000340.2:c.581T>G
MANE Select
|
NP_000331.1:p.Leu194Arg
|
|
NM_001278658.2:c.224T>G
|
NP_001265587.1:p.Leu75Arg
|
|
NM_001278659.2:c.62T>G
|
NP_001265588.1:p.Leu21Arg
|
|