ENST00000413910.6:c.981G>T
|
ENSP00000400542.2:p.Lys327Asn
|
|
ENST00000426673.6:c.*484G>T
|
ENSP00000407253.3:n.*484G>T
|
|
ENST00000484317.6:n.886G>T
|
|
|
ENST00000696575.1:c.1101G>T
|
ENSP00000512730.1:p.Lys367Asn
|
|
ENST00000696577.1:c.1101G>T
|
ENSP00000512731.1:p.Lys367Asn
|
|
ENST00000696578.1:c.*53G>T
|
ENSP00000512732.1:n.*53G>T
|
|
ENST00000696579.1:n.1203G>T
|
|
|
ENST00000696580.1:c.1014G>T
|
ENSP00000512733.1:p.Lys338Asn
|
|
ENST00000696581.1:c.*1075G>T
|
ENSP00000512734.1:n.*1075G>T
|
|
ENST00000696582.1:c.*307G>T
|
ENSP00000512735.1:n.*307G>T
|
|
ENST00000696583.1:c.1062G>T
|
ENSP00000512736.1:p.Lys354Asn
|
|
ENST00000696584.1:n.1625G>T
|
|
|
ENST00000696585.1:n.1744G>T
|
|
|
ENST00000696586.1:n.1518G>T
|
|
|
ENST00000696587.1:c.981G>T
|
ENSP00000512737.1:p.Lys327Asn
|
|
ENST00000696588.1:c.492G>T
|
ENSP00000513251.1:p.Lys164Asn
|
|
ENST00000696589.1:n.876G>T
|
|
|
ENST00000696590.1:n.725G>T
|
|
|
ENST00000696591.1:n.450G>T
|
|
|
ENST00000696592.1:n.1980G>T
|
|
|
ENST00000696627.1:c.1101G>T
|
ENSP00000512764.1:p.Lys367Asn
|
|
ENST00000696628.1:c.1101G>T
|
ENSP00000512765.1:p.Lys367Asn
|
|
ENST00000369550.10:c.1101G>T
MANE Select
|
ENSP00000358563.5:p.Lys367Asn
|
|
ENST00000369550.9:c.1101G>T
|
ENSP00000358563.5:p.Lys367Asn
|
|
ENST00000412124.5:c.359G>T
|
|
|
ENST00000426673.5:c.461G>T
|
|
|
ENST00000475966.1:n.590G>T
|
|
|
ENST00000481062.1:n.52G>T
|
|
|
ENST00000620277.4:c.1101G>T
|
ENSP00000478387.1:p.Lys367Asn
|
|
NM_001142463.2:c.1101G>T
|
NP_001135935.1:p.Lys367Asn
|
|
NM_001288747.1:c.1101G>T
|
NP_001275676.1:p.Lys367Asn
|
|
NM_001363.4:c.1101G>T
|
NP_001354.1:p.Lys367Asn
|
|
NR_110021.1:n.1802G>T
|
|
|
NR_110022.1:n.1921G>T
|
|
|
NR_110023.1:n.1695G>T
|
|
|
NM_001363.5:c.1101G>T
MANE Select
|
NP_001354.1:p.Lys367Asn
|
|
NM_001142463.3:c.1101G>T
|
NP_001135935.1:p.Lys367Asn
|
|
NR_110021.2:n.1680G>T
|
|
|
NR_110022.2:n.1799G>T
|
|
|
NR_110023.2:n.1573G>T
|
|
|
NM_001288747.2:c.1101G>T
|
NP_001275676.1:p.Lys367Asn
|
|