|
ENST00000247138.11:c.468C>G
MANE Select
|
ENSP00000247138.5:p.Ser156=
|
|
|
ENST00000247138.10:c.468C>G
|
ENSP00000247138.5:p.Ser156=
|
|
|
ENST00000376515.8:c.355-549C>G
|
ENSP00000365698.3:n.355-549C>G
|
|
|
ENST00000376521.6:c.468C>G
|
ENSP00000365704.1:p.Ser156=
|
|
|
ENST00000376529.8:c.427-549C>G
|
ENSP00000365712.3:n.427-549C>G
|
|
|
ENST00000413561.7:c.212-182C>G
|
|
|
|
ENST00000445167.7:c.427-549C>G
|
ENSP00000402726.2:n.427-549C>G
|
|
|
ENST00000446885.1:c.252C>G
|
ENSP00000415518.1:p.Ser84=
|
|
|
ENST00000452555.7:c.552C>G
|
ENSP00000416002.2:p.Ser184=
|
|
|
ENST00000616181.5:c.507C>G
|
ENSP00000478617.1:p.Ser169=
|
|
|
ENST00000634665.1:c.*88C>G
|
ENSP00000489356.1:n.*88C>G
|
|
|
ENST00000635238.1:c.429C>G
|
ENSP00000489515.1:p.Ser143=
|
|
|
ENST00000635285.1:c.468C>G
|
ENSP00000489484.1:p.Ser156=
|
|
|
ENST00000635460.1:c.424+951C>G
|
|
|
|
ENST00000635589.1:c.285C>G
|
ENSP00000489197.1:p.Ser95=
|
|
|
ENST00000635628.1:c.*362C>G
|
ENSP00000489613.1:n.*362C>G
|
|
|
NM_001032289.2:c.427-549C>G
|
NP_001027460.1:n.427-549C>G
|
|
|
NM_001042498.2:c.468C>G
|
NP_001035963.1:p.Ser156=
|
|
|
NM_001282647.1:c.427-549C>G
|
NP_001269576.1:n.427-549C>G
|
|
|
NM_001282648.1:c.355-549C>G
|
NP_001269577.1:n.355-549C>G
|
|
|
NM_001282649.1:c.285C>G
|
NP_001269578.1:p.Ser95=
|
|
|
NM_001282650.1:c.507C>G
|
NP_001269579.1:p.Ser169=
|
|
|
NM_001282651.1:c.552C>G
|
NP_001269580.1:p.Ser184=
|
|
|
NM_005660.2:c.468C>G
|
NP_005651.1:p.Ser156=
|
|
|
NM_005660.3:c.468C>G
MANE Select
|
NP_005651.1:p.Ser156=
|
|
|
NM_001032289.3:c.427-549C>G
|
NP_001027460.1:n.427-549C>G
|
|
|
NM_001042498.3:c.468C>G
|
NP_001035963.1:p.Ser156=
|
|
|
NM_001282647.2:c.427-549C>G
|
NP_001269576.1:n.427-549C>G
|
|
|
NM_001282649.2:c.285C>G
|
NP_001269578.1:p.Ser95=
|
|
|
NM_001282650.2:c.507C>G
|
NP_001269579.1:p.Ser169=
|
|
|
NM_001282651.2:c.552C>G
|
NP_001269580.1:p.Ser184=
|
|
|
NM_001282648.2:c.355-549C>G
|
NP_001269577.1:n.355-549C>G
|
|
