ENST00000355943.8:c.1239T>G
MANE Select
|
ENSP00000348211.3:p.Leu413=
|
|
ENST00000355943.7:c.1239T>G
|
ENSP00000348211.3:p.Leu413=
|
|
ENST00000447245.6:c.996T>G
|
ENSP00000399717.2:p.Leu332=
|
|
ENST00000504098.1:c.801T>G
|
ENSP00000425708.1:p.Leu267=
|
|
ENST00000509432.1:c.600T>G
|
ENSP00000426604.1:p.Leu200=
|
|
ENST00000513706.2:n.2839T>G
|
|
|
ENST00000513807.5:c.753T>G
|
ENSP00000421134.1:p.Leu251=
|
|
NM_001303249.1:c.996T>G
|
NP_001290178.1:p.Leu332=
|
|
NM_001303250.1:c.966T>G
|
NP_001290179.1:p.Leu322=
|
|
NM_138773.2:c.1239T>G
|
NP_620128.1:p.Leu413=
|
|
NM_001303249.2:c.996T>G
|
NP_001290178.1:p.Leu332=
|
|
NM_001303250.2:c.966T>G
|
NP_001290179.1:p.Leu322=
|
|
NM_138773.3:c.1239T>G
|
NP_620128.1:p.Leu413=
|
|
NR_138151.1:n.1513T>G
|
|
|
NM_138773.4:c.1239T>G
MANE Select
|
NP_620128.1:p.Leu413=
|
|
NM_001303249.3:c.996T>G
|
NP_001290178.1:p.Leu332=
|
|
NM_001303250.3:c.966T>G
|
NP_001290179.1:p.Leu322=
|
|
NR_138151.2:n.1478T>G
|
|
|