ENST00000413910.6:c.1004C>T
|
ENSP00000400542.2:p.Thr335Ile
|
|
ENST00000426673.6:c.*507C>T
|
ENSP00000407253.3:n.*507C>T
|
|
ENST00000484317.6:n.909C>T
|
|
|
ENST00000696575.1:c.1124C>T
|
ENSP00000512730.1:p.Thr375Ile
|
|
ENST00000696577.1:c.1124C>T
|
ENSP00000512731.1:p.Thr375Ile
|
|
ENST00000696578.1:c.*76C>T
|
ENSP00000512732.1:n.*76C>T
|
|
ENST00000696579.1:n.1226C>T
|
|
|
ENST00000696580.1:c.1037C>T
|
ENSP00000512733.1:p.Thr346Ile
|
|
ENST00000696581.1:c.*1098C>T
|
ENSP00000512734.1:n.*1098C>T
|
|
ENST00000696582.1:c.*330C>T
|
ENSP00000512735.1:n.*330C>T
|
|
ENST00000696583.1:c.1085C>T
|
ENSP00000512736.1:p.Thr362Ile
|
|
ENST00000696584.1:n.1648C>T
|
|
|
ENST00000696585.1:n.1767C>T
|
|
|
ENST00000696586.1:n.1541C>T
|
|
|
ENST00000696587.1:c.1004C>T
|
ENSP00000512737.1:p.Thr335Ile
|
|
ENST00000696588.1:c.515C>T
|
ENSP00000513251.1:p.Thr172Ile
|
|
ENST00000696589.1:n.899C>T
|
|
|
ENST00000696590.1:n.748C>T
|
|
|
ENST00000696591.1:n.473C>T
|
|
|
ENST00000696592.1:n.2003C>T
|
|
|
ENST00000696627.1:c.1124C>T
|
ENSP00000512764.1:p.Thr375Ile
|
|
ENST00000696628.1:c.1124C>T
|
ENSP00000512765.1:p.Thr375Ile
|
|
ENST00000369550.10:c.1124C>T
MANE Select
|
ENSP00000358563.5:p.Thr375Ile
|
|
ENST00000369550.9:c.1124C>T
|
ENSP00000358563.5:p.Thr375Ile
|
|
ENST00000412124.5:c.382C>T
|
|
|
ENST00000426673.5:c.484C>T
|
|
|
ENST00000475966.1:n.613C>T
|
|
|
ENST00000481062.1:n.75C>T
|
|
|
ENST00000620277.4:c.1124C>T
|
ENSP00000478387.1:p.Thr375Ile
|
|
NM_001142463.2:c.1124C>T
|
NP_001135935.1:p.Thr375Ile
|
|
NM_001288747.1:c.1124C>T
|
NP_001275676.1:p.Thr375Ile
|
|
NM_001363.4:c.1124C>T
|
NP_001354.1:p.Thr375Ile
|
|
NR_110021.1:n.1825C>T
|
|
|
NR_110022.1:n.1944C>T
|
|
|
NR_110023.1:n.1718C>T
|
|
|
NM_001363.5:c.1124C>T
MANE Select
|
NP_001354.1:p.Thr375Ile
|
|
NM_001142463.3:c.1124C>T
|
NP_001135935.1:p.Thr375Ile
|
|
NR_110021.2:n.1703C>T
|
|
|
NR_110022.2:n.1822C>T
|
|
|
NR_110023.2:n.1596C>T
|
|
|
NM_001288747.2:c.1124C>T
|
NP_001275676.1:p.Thr375Ile
|
|