ENST00000355943.8:c.1241T>G
MANE Select
|
ENSP00000348211.3:p.Leu414Arg
|
|
ENST00000355943.7:c.1241T>G
|
ENSP00000348211.3:p.Leu414Arg
|
|
ENST00000447245.6:c.998T>G
|
ENSP00000399717.2:p.Leu333Arg
|
|
ENST00000504098.1:c.803T>G
|
ENSP00000425708.1:p.Leu268Arg
|
|
ENST00000509432.1:c.602T>G
|
ENSP00000426604.1:p.Leu201Arg
|
|
ENST00000513706.2:n.2841T>G
|
|
|
ENST00000513807.5:c.755T>G
|
ENSP00000421134.1:p.Leu252Arg
|
|
NM_001303249.1:c.998T>G
|
NP_001290178.1:p.Leu333Arg
|
|
NM_001303250.1:c.968T>G
|
NP_001290179.1:p.Leu323Arg
|
|
NM_138773.2:c.1241T>G
|
NP_620128.1:p.Leu414Arg
|
|
NM_001303249.2:c.998T>G
|
NP_001290178.1:p.Leu333Arg
|
|
NM_001303250.2:c.968T>G
|
NP_001290179.1:p.Leu323Arg
|
|
NM_138773.3:c.1241T>G
|
NP_620128.1:p.Leu414Arg
|
|
NR_138151.1:n.1515T>G
|
|
|
NM_138773.4:c.1241T>G
MANE Select
|
NP_620128.1:p.Leu414Arg
|
|
NM_001303249.3:c.998T>G
|
NP_001290178.1:p.Leu333Arg
|
|
NM_001303250.3:c.968T>G
|
NP_001290179.1:p.Leu323Arg
|
|
NR_138151.2:n.1480T>G
|
|
|