ENST00000413910.6:c.652-99G>T
|
ENSP00000400542.2:n.652-99G>T
|
|
ENST00000426673.6:c.*155-99G>T
|
ENSP00000407253.3:n.*155-99G>T
|
|
ENST00000484317.6:n.557-99G>T
|
|
|
ENST00000696575.1:c.772-99G>T
|
ENSP00000512730.1:n.772-99G>T
|
|
ENST00000696576.1:n.874-99G>T
|
|
|
ENST00000696577.1:c.772-99G>T
|
ENSP00000512731.1:n.772-99G>T
|
|
ENST00000696578.1:c.772-99G>T
|
ENSP00000512732.1:n.772-99G>T
|
|
ENST00000696579.1:n.874-99G>T
|
|
|
ENST00000696580.1:c.685-99G>T
|
ENSP00000512733.1:n.685-99G>T
|
|
ENST00000696581.1:c.*746-99G>T
|
ENSP00000512734.1:n.*746-99G>T
|
|
ENST00000696582.1:c.641-99G>T
|
ENSP00000512735.1:n.641-99G>T
|
|
ENST00000696583.1:c.772-138G>T
|
ENSP00000512736.1:n.772-138G>T
|
|
ENST00000696584.1:n.1296-99G>T
|
|
|
ENST00000696585.1:n.1415-99G>T
|
|
|
ENST00000696586.1:n.1189-99G>T
|
|
|
ENST00000696587.1:c.652-99G>T
|
ENSP00000512737.1:n.652-99G>T
|
|
ENST00000696588.1:c.163-99G>T
|
ENSP00000513251.1:n.163-99G>T
|
|
ENST00000696589.1:n.547-99G>T
|
|
|
ENST00000696590.1:n.396-99G>T
|
|
|
ENST00000696591.1:n.22G>T
|
|
|
ENST00000696627.1:c.772-99G>T
|
ENSP00000512764.1:n.772-99G>T
|
|
ENST00000696628.1:c.772-99G>T
|
ENSP00000512765.1:n.772-99G>T
|
|
ENST00000369550.10:c.772-99G>T
MANE Select
|
ENSP00000358563.5:n.772-99G>T
|
|
ENST00000369550.9:c.772-99G>T
|
ENSP00000358563.5:n.772-99G>T
|
|
ENST00000412124.5:c.173+1686G>T
|
|
|
ENST00000413910.5:c.652-99G>T
|
ENSP00000400542.1:n.652-99G>T
|
|
ENST00000426673.5:c.132-99G>T
|
|
|
ENST00000452771.5:c.665-99G>T
|
ENSP00000407325.1:n.665-99G>T
|
|
ENST00000475966.1:n.261-99G>T
|
|
|
ENST00000484317.5:n.410-99G>T
|
|
|
ENST00000620277.4:c.772-99G>T
|
ENSP00000478387.1:n.772-99G>T
|
|
NM_001142463.2:c.772-99G>T
|
NP_001135935.1:n.772-99G>T
|
|
NM_001288747.1:c.772-99G>T
|
NP_001275676.1:n.772-99G>T
|
|
NM_001363.4:c.772-99G>T
|
NP_001354.1:n.772-99G>T
|
|
NR_110021.1:n.1473-99G>T
|
|
|
NR_110022.1:n.1592-99G>T
|
|
|
NR_110023.1:n.1366-99G>T
|
|
|
NM_001363.5:c.772-99G>T
MANE Select
|
NP_001354.1:n.772-99G>T
|
|
NM_001142463.3:c.772-99G>T
|
NP_001135935.1:n.772-99G>T
|
|
NR_110021.2:n.1351-99G>T
|
|
|
NR_110022.2:n.1470-99G>T
|
|
|
NR_110023.2:n.1244-99G>T
|
|
|
NM_001288747.2:c.772-99G>T
|
NP_001275676.1:n.772-99G>T
|
|