|
ENST00000247138.11:c.532G>T
MANE Select
|
ENSP00000247138.5:p.Gly178Cys
|
|
|
ENST00000247138.10:c.532G>T
|
ENSP00000247138.5:p.Gly178Cys
|
|
|
ENST00000376515.8:c.355-485G>T
|
ENSP00000365698.3:n.355-485G>T
|
|
|
ENST00000376521.6:c.532G>T
|
ENSP00000365704.1:p.Gly178Cys
|
|
|
ENST00000376529.8:c.427-485G>T
|
ENSP00000365712.3:n.427-485G>T
|
|
|
ENST00000413561.7:c.212-118G>T
|
|
|
|
ENST00000445167.7:c.427-485G>T
|
ENSP00000402726.2:n.427-485G>T
|
|
|
ENST00000446885.1:c.316G>T
|
ENSP00000415518.1:p.Gly106Cys
|
|
|
ENST00000452555.7:c.616G>T
|
ENSP00000416002.2:p.Gly206Cys
|
|
|
ENST00000616181.5:c.571G>T
|
ENSP00000478617.1:p.Gly191Cys
|
|
|
ENST00000635238.1:c.493G>T
|
ENSP00000489515.1:p.Gly165Cys
|
|
|
ENST00000635285.1:c.532G>T
|
ENSP00000489484.1:p.Gly178Cys
|
|
|
ENST00000635460.1:c.424+1015G>T
|
|
|
|
ENST00000635589.1:c.349G>T
|
ENSP00000489197.1:p.Gly117Cys
|
|
|
ENST00000635628.1:c.*426G>T
|
ENSP00000489613.1:n.*426G>T
|
|
|
NM_001032289.2:c.427-485G>T
|
NP_001027460.1:n.427-485G>T
|
|
|
NM_001042498.2:c.532G>T
|
NP_001035963.1:p.Gly178Cys
|
|
|
NM_001282647.1:c.427-485G>T
|
NP_001269576.1:n.427-485G>T
|
|
|
NM_001282648.1:c.355-485G>T
|
NP_001269577.1:n.355-485G>T
|
|
|
NM_001282649.1:c.349G>T
|
NP_001269578.1:p.Gly117Cys
|
|
|
NM_001282650.1:c.571G>T
|
NP_001269579.1:p.Gly191Cys
|
|
|
NM_001282651.1:c.616G>T
|
NP_001269580.1:p.Gly206Cys
|
|
|
NM_005660.2:c.532G>T
|
NP_005651.1:p.Gly178Cys
|
|
|
NM_005660.3:c.532G>T
MANE Select
|
NP_005651.1:p.Gly178Cys
|
|
|
NM_001032289.3:c.427-485G>T
|
NP_001027460.1:n.427-485G>T
|
|
|
NM_001042498.3:c.532G>T
|
NP_001035963.1:p.Gly178Cys
|
|
|
NM_001282647.2:c.427-485G>T
|
NP_001269576.1:n.427-485G>T
|
|
|
NM_001282649.2:c.349G>T
|
NP_001269578.1:p.Gly117Cys
|
|
|
NM_001282650.2:c.571G>T
|
NP_001269579.1:p.Gly191Cys
|
|
|
NM_001282651.2:c.616G>T
|
NP_001269580.1:p.Gly206Cys
|
|
|
NM_001282648.2:c.355-485G>T
|
NP_001269577.1:n.355-485G>T
|
|
