ENST00000413910.6:c.726G>T
|
ENSP00000400542.2:p.Leu242=
|
|
ENST00000426673.6:c.*229G>T
|
ENSP00000407253.3:n.*229G>T
|
|
ENST00000484317.6:n.631G>T
|
|
|
ENST00000696575.1:c.846G>T
|
ENSP00000512730.1:p.Leu282=
|
|
ENST00000696576.1:n.948G>T
|
|
|
ENST00000696577.1:c.846G>T
|
ENSP00000512731.1:p.Leu282=
|
|
ENST00000696578.1:c.846G>T
|
ENSP00000512732.1:p.Leu282=
|
|
ENST00000696579.1:n.948G>T
|
|
|
ENST00000696580.1:c.759G>T
|
ENSP00000512733.1:p.Leu253=
|
|
ENST00000696581.1:c.*820G>T
|
ENSP00000512734.1:n.*820G>T
|
|
ENST00000696582.1:c.*52G>T
|
ENSP00000512735.1:n.*52G>T
|
|
ENST00000696583.1:c.807G>T
|
ENSP00000512736.1:p.Leu269=
|
|
ENST00000696584.1:n.1370G>T
|
|
|
ENST00000696585.1:n.1489G>T
|
|
|
ENST00000696586.1:n.1263G>T
|
|
|
ENST00000696587.1:c.726G>T
|
ENSP00000512737.1:p.Leu242=
|
|
ENST00000696588.1:c.237G>T
|
ENSP00000513251.1:p.Leu79=
|
|
ENST00000696589.1:n.621G>T
|
|
|
ENST00000696590.1:n.470G>T
|
|
|
ENST00000696591.1:n.195G>T
|
|
|
ENST00000696627.1:c.846G>T
|
ENSP00000512764.1:p.Leu282=
|
|
ENST00000696628.1:c.846G>T
|
ENSP00000512765.1:p.Leu282=
|
|
ENST00000369550.10:c.846G>T
MANE Select
|
ENSP00000358563.5:p.Leu282=
|
|
ENST00000369550.9:c.846G>T
|
ENSP00000358563.5:p.Leu282=
|
|
ENST00000412124.5:c.174-1518G>T
|
|
|
ENST00000413910.5:c.726G>T
|
ENSP00000400542.1:p.Leu242=
|
|
ENST00000426673.5:c.206G>T
|
|
|
ENST00000475966.1:n.335G>T
|
|
|
ENST00000484317.5:n.484G>T
|
|
|
ENST00000620277.4:c.846G>T
|
ENSP00000478387.1:p.Leu282=
|
|
NM_001142463.2:c.846G>T
|
NP_001135935.1:p.Leu282=
|
|
NM_001288747.1:c.846G>T
|
NP_001275676.1:p.Leu282=
|
|
NM_001363.4:c.846G>T
|
NP_001354.1:p.Leu282=
|
|
NR_110021.1:n.1547G>T
|
|
|
NR_110022.1:n.1666G>T
|
|
|
NR_110023.1:n.1440G>T
|
|
|
NM_001363.5:c.846G>T
MANE Select
|
NP_001354.1:p.Leu282=
|
|
NM_001142463.3:c.846G>T
|
NP_001135935.1:p.Leu282=
|
|
NR_110021.2:n.1425G>T
|
|
|
NR_110022.2:n.1544G>T
|
|
|
NR_110023.2:n.1318G>T
|
|
|
NM_001288747.2:c.846G>T
|
NP_001275676.1:p.Leu282=
|
|