ENST00000413910.6:c.752A>T
|
ENSP00000400542.2:p.Lys251Met
|
|
ENST00000426673.6:c.*255A>T
|
ENSP00000407253.3:n.*255A>T
|
|
ENST00000484317.6:n.657A>T
|
|
|
ENST00000696575.1:c.872A>T
|
ENSP00000512730.1:p.Lys291Met
|
|
ENST00000696576.1:n.974A>T
|
|
|
ENST00000696577.1:c.872A>T
|
ENSP00000512731.1:p.Lys291Met
|
|
ENST00000696578.1:c.872A>T
|
ENSP00000512732.1:p.Lys291Met
|
|
ENST00000696579.1:n.974A>T
|
|
|
ENST00000696580.1:c.785A>T
|
ENSP00000512733.1:p.Lys262Met
|
|
ENST00000696581.1:c.*846A>T
|
ENSP00000512734.1:n.*846A>T
|
|
ENST00000696582.1:c.*78A>T
|
ENSP00000512735.1:n.*78A>T
|
|
ENST00000696583.1:c.833A>T
|
ENSP00000512736.1:p.Lys278Met
|
|
ENST00000696584.1:n.1396A>T
|
|
|
ENST00000696585.1:n.1515A>T
|
|
|
ENST00000696586.1:n.1289A>T
|
|
|
ENST00000696587.1:c.752A>T
|
ENSP00000512737.1:p.Lys251Met
|
|
ENST00000696588.1:c.263A>T
|
ENSP00000513251.1:p.Lys88Met
|
|
ENST00000696589.1:n.647A>T
|
|
|
ENST00000696590.1:n.496A>T
|
|
|
ENST00000696591.1:n.221A>T
|
|
|
ENST00000696627.1:c.872A>T
|
ENSP00000512764.1:p.Lys291Met
|
|
ENST00000696628.1:c.872A>T
|
ENSP00000512765.1:p.Lys291Met
|
|
ENST00000369550.10:c.872A>T
MANE Select
|
ENSP00000358563.5:p.Lys291Met
|
|
ENST00000369550.9:c.872A>T
|
ENSP00000358563.5:p.Lys291Met
|
|
ENST00000412124.5:c.174-1492A>T
|
|
|
ENST00000413910.5:c.752A>T
|
ENSP00000400542.1:p.Lys251Met
|
|
ENST00000426673.5:c.232A>T
|
|
|
ENST00000475966.1:n.361A>T
|
|
|
ENST00000484317.5:n.510A>T
|
|
|
ENST00000620277.4:c.872A>T
|
ENSP00000478387.1:p.Lys291Met
|
|
NM_001142463.2:c.872A>T
|
NP_001135935.1:p.Lys291Met
|
|
NM_001288747.1:c.872A>T
|
NP_001275676.1:p.Lys291Met
|
|
NM_001363.4:c.872A>T
|
NP_001354.1:p.Lys291Met
|
|
NR_110021.1:n.1573A>T
|
|
|
NR_110022.1:n.1692A>T
|
|
|
NR_110023.1:n.1466A>T
|
|
|
NM_001363.5:c.872A>T
MANE Select
|
NP_001354.1:p.Lys291Met
|
|
NM_001142463.3:c.872A>T
|
NP_001135935.1:p.Lys291Met
|
|
NR_110021.2:n.1451A>T
|
|
|
NR_110022.2:n.1570A>T
|
|
|
NR_110023.2:n.1344A>T
|
|
|
NM_001288747.2:c.872A>T
|
NP_001275676.1:p.Lys291Met
|
|