ENST00000413910.6:c.980A>C
|
ENSP00000400542.2:p.Lys327Thr
|
|
ENST00000426673.6:c.*483A>C
|
ENSP00000407253.3:n.*483A>C
|
|
ENST00000484317.6:n.885A>C
|
|
|
ENST00000696575.1:c.1100A>C
|
ENSP00000512730.1:p.Lys367Thr
|
|
ENST00000696577.1:c.1100A>C
|
ENSP00000512731.1:p.Lys367Thr
|
|
ENST00000696578.1:c.*52A>C
|
ENSP00000512732.1:n.*52A>C
|
|
ENST00000696579.1:n.1202A>C
|
|
|
ENST00000696580.1:c.1013A>C
|
ENSP00000512733.1:p.Lys338Thr
|
|
ENST00000696581.1:c.*1074A>C
|
ENSP00000512734.1:n.*1074A>C
|
|
ENST00000696582.1:c.*306A>C
|
ENSP00000512735.1:n.*306A>C
|
|
ENST00000696583.1:c.1061A>C
|
ENSP00000512736.1:p.Lys354Thr
|
|
ENST00000696584.1:n.1624A>C
|
|
|
ENST00000696585.1:n.1743A>C
|
|
|
ENST00000696586.1:n.1517A>C
|
|
|
ENST00000696587.1:c.980A>C
|
ENSP00000512737.1:p.Lys327Thr
|
|
ENST00000696588.1:c.491A>C
|
ENSP00000513251.1:p.Lys164Thr
|
|
ENST00000696589.1:n.875A>C
|
|
|
ENST00000696590.1:n.724A>C
|
|
|
ENST00000696591.1:n.449A>C
|
|
|
ENST00000696592.1:n.1979A>C
|
|
|
ENST00000696627.1:c.1100A>C
|
ENSP00000512764.1:p.Lys367Thr
|
|
ENST00000696628.1:c.1100A>C
|
ENSP00000512765.1:p.Lys367Thr
|
|
ENST00000369550.10:c.1100A>C
MANE Select
|
ENSP00000358563.5:p.Lys367Thr
|
|
ENST00000369550.9:c.1100A>C
|
ENSP00000358563.5:p.Lys367Thr
|
|
ENST00000412124.5:c.358A>C
|
|
|
ENST00000426673.5:c.460A>C
|
|
|
ENST00000475966.1:n.589A>C
|
|
|
ENST00000481062.1:n.51A>C
|
|
|
ENST00000620277.4:c.1100A>C
|
ENSP00000478387.1:p.Lys367Thr
|
|
NM_001142463.2:c.1100A>C
|
NP_001135935.1:p.Lys367Thr
|
|
NM_001288747.1:c.1100A>C
|
NP_001275676.1:p.Lys367Thr
|
|
NM_001363.4:c.1100A>C
|
NP_001354.1:p.Lys367Thr
|
|
NR_110021.1:n.1801A>C
|
|
|
NR_110022.1:n.1920A>C
|
|
|
NR_110023.1:n.1694A>C
|
|
|
NM_001363.5:c.1100A>C
MANE Select
|
NP_001354.1:p.Lys367Thr
|
|
NM_001142463.3:c.1100A>C
|
NP_001135935.1:p.Lys367Thr
|
|
NR_110021.2:n.1679A>C
|
|
|
NR_110022.2:n.1798A>C
|
|
|
NR_110023.2:n.1572A>C
|
|
|
NM_001288747.2:c.1100A>C
|
NP_001275676.1:p.Lys367Thr
|
|