ENST00000413910.6:c.1027G>T
|
ENSP00000400542.2:p.Gly343Cys
|
|
ENST00000426673.6:c.*530G>T
|
ENSP00000407253.3:n.*530G>T
|
|
ENST00000484317.6:n.932G>T
|
|
|
ENST00000696575.1:c.1147G>T
|
ENSP00000512730.1:p.Gly383Cys
|
|
ENST00000696577.1:c.1147G>T
|
ENSP00000512731.1:p.Gly383Cys
|
|
ENST00000696578.1:c.*99G>T
|
ENSP00000512732.1:n.*99G>T
|
|
ENST00000696579.1:n.1249G>T
|
|
|
ENST00000696580.1:c.1060G>T
|
ENSP00000512733.1:p.Gly354Cys
|
|
ENST00000696581.1:c.*1121G>T
|
ENSP00000512734.1:n.*1121G>T
|
|
ENST00000696582.1:c.*353G>T
|
ENSP00000512735.1:n.*353G>T
|
|
ENST00000696583.1:c.1108G>T
|
ENSP00000512736.1:p.Gly370Cys
|
|
ENST00000696584.1:n.1671G>T
|
|
|
ENST00000696585.1:n.1790G>T
|
|
|
ENST00000696586.1:n.1564G>T
|
|
|
ENST00000696587.1:c.1027G>T
|
ENSP00000512737.1:p.Gly343Cys
|
|
ENST00000696588.1:c.538G>T
|
ENSP00000513251.1:p.Gly180Cys
|
|
ENST00000696589.1:n.922G>T
|
|
|
ENST00000696590.1:n.771G>T
|
|
|
ENST00000696591.1:n.496G>T
|
|
|
ENST00000696592.1:n.2026G>T
|
|
|
ENST00000696627.1:c.1147G>T
|
ENSP00000512764.1:p.Gly383Cys
|
|
ENST00000696628.1:c.1147G>T
|
ENSP00000512765.1:p.Gly383Cys
|
|
ENST00000369550.10:c.1147G>T
MANE Select
|
ENSP00000358563.5:p.Gly383Cys
|
|
ENST00000369550.9:c.1147G>T
|
ENSP00000358563.5:p.Gly383Cys
|
|
ENST00000412124.5:c.405G>T
|
|
|
ENST00000426673.5:c.507G>T
|
|
|
ENST00000475966.1:n.636G>T
|
|
|
ENST00000481062.1:n.98G>T
|
|
|
ENST00000620277.4:c.1147G>T
|
ENSP00000478387.1:p.Gly383Cys
|
|
NM_001142463.2:c.1147G>T
|
NP_001135935.1:p.Gly383Cys
|
|
NM_001288747.1:c.1147G>T
|
NP_001275676.1:p.Gly383Cys
|
|
NM_001363.4:c.1147G>T
|
NP_001354.1:p.Gly383Cys
|
|
NR_110021.1:n.1848G>T
|
|
|
NR_110022.1:n.1967G>T
|
|
|
NR_110023.1:n.1741G>T
|
|
|
NM_001363.5:c.1147G>T
MANE Select
|
NP_001354.1:p.Gly383Cys
|
|
NM_001142463.3:c.1147G>T
|
NP_001135935.1:p.Gly383Cys
|
|
NR_110021.2:n.1726G>T
|
|
|
NR_110022.2:n.1845G>T
|
|
|
NR_110023.2:n.1619G>T
|
|
|
NM_001288747.2:c.1147G>T
|
NP_001275676.1:p.Gly383Cys
|
|