ENST00000413910.6:c.723C>A
|
ENSP00000400542.2:p.Tyr241Ter
|
|
ENST00000426673.6:c.*226C>A
|
ENSP00000407253.3:n.*226C>A
|
|
ENST00000484317.6:n.628C>A
|
|
|
ENST00000696575.1:c.843C>A
|
ENSP00000512730.1:p.Tyr281Ter
|
|
ENST00000696576.1:n.945C>A
|
|
|
ENST00000696577.1:c.843C>A
|
ENSP00000512731.1:p.Tyr281Ter
|
|
ENST00000696578.1:c.843C>A
|
ENSP00000512732.1:p.Tyr281Ter
|
|
ENST00000696579.1:n.945C>A
|
|
|
ENST00000696580.1:c.756C>A
|
ENSP00000512733.1:p.Tyr252Ter
|
|
ENST00000696581.1:c.*817C>A
|
ENSP00000512734.1:n.*817C>A
|
|
ENST00000696582.1:c.*49C>A
|
ENSP00000512735.1:n.*49C>A
|
|
ENST00000696583.1:c.804C>A
|
ENSP00000512736.1:p.Tyr268Ter
|
|
ENST00000696584.1:n.1367C>A
|
|
|
ENST00000696585.1:n.1486C>A
|
|
|
ENST00000696586.1:n.1260C>A
|
|
|
ENST00000696587.1:c.723C>A
|
ENSP00000512737.1:p.Tyr241Ter
|
|
ENST00000696588.1:c.234C>A
|
ENSP00000513251.1:p.Tyr78Ter
|
|
ENST00000696589.1:n.618C>A
|
|
|
ENST00000696590.1:n.467C>A
|
|
|
ENST00000696591.1:n.192C>A
|
|
|
ENST00000696627.1:c.843C>A
|
ENSP00000512764.1:p.Tyr281Ter
|
|
ENST00000696628.1:c.843C>A
|
ENSP00000512765.1:p.Tyr281Ter
|
|
ENST00000369550.10:c.843C>A
MANE Select
|
ENSP00000358563.5:p.Tyr281Ter
|
|
ENST00000369550.9:c.843C>A
|
ENSP00000358563.5:p.Tyr281Ter
|
|
ENST00000412124.5:c.174-1521C>A
|
|
|
ENST00000413910.5:c.723C>A
|
ENSP00000400542.1:p.Tyr241Ter
|
|
ENST00000426673.5:c.203C>A
|
|
|
ENST00000475966.1:n.332C>A
|
|
|
ENST00000484317.5:n.481C>A
|
|
|
ENST00000620277.4:c.843C>A
|
ENSP00000478387.1:p.Tyr281Ter
|
|
NM_001142463.2:c.843C>A
|
NP_001135935.1:p.Tyr281Ter
|
|
NM_001288747.1:c.843C>A
|
NP_001275676.1:p.Tyr281Ter
|
|
NM_001363.4:c.843C>A
|
NP_001354.1:p.Tyr281Ter
|
|
NR_110021.1:n.1544C>A
|
|
|
NR_110022.1:n.1663C>A
|
|
|
NR_110023.1:n.1437C>A
|
|
|
NM_001363.5:c.843C>A
MANE Select
|
NP_001354.1:p.Tyr281Ter
|
|
NM_001142463.3:c.843C>A
|
NP_001135935.1:p.Tyr281Ter
|
|
NR_110021.2:n.1422C>A
|
|
|
NR_110022.2:n.1541C>A
|
|
|
NR_110023.2:n.1315C>A
|
|
|
NM_001288747.2:c.843C>A
|
NP_001275676.1:p.Tyr281Ter
|
|