ENST00000366159.9:n.2125G>T
|
|
|
ENST00000437813.8:c.*485G>T
|
ENSP00000513672.1:n.*485G>T
|
|
ENST00000440083.7:c.1243G>T
|
ENSP00000413224.3:p.Glu415Ter
|
|
ENST00000535958.2:c.*851G>T
|
ENSP00000513673.1:n.*851G>T
|
|
ENST00000698337.1:n.985G>T
|
|
|
ENST00000698338.1:n.1638G>T
|
|
|
ENST00000698339.1:c.*519G>T
|
ENSP00000513670.1:n.*519G>T
|
|
ENST00000698340.1:c.*263G>T
|
ENSP00000513671.1:n.*263G>T
|
|
ENST00000162749.7:c.1024G>T
MANE Select
|
ENSP00000162749.2:p.Glu342Ter
|
|
ENST00000162749.6:c.1024G>T
|
ENSP00000162749.2:p.Glu342Ter
|
|
ENST00000534885.5:c.*501G>T
|
ENSP00000441803.1:n.*501G>T
|
|
ENST00000536717.5:n.928G>T
|
|
|
ENST00000540022.5:c.895G>T
|
ENSP00000438343.1:p.Glu299Ter
|
|
ENST00000543359.5:n.436G>T
|
|
|
ENST00000543995.5:c.*611G>T
|
ENSP00000442405.1:n.*611G>T
|
|
NM_001065.3:c.1024G>T , LRG_193t1:c.1024G>T
|
NP_001056.1:p.Glu342Ter
|
|
NM_001346091.1:c.700G>T
|
NP_001333020.1:p.Glu234Ter
|
|
NM_001346092.1:c.565G>T
|
NP_001333021.1:p.Glu189Ter
|
|
NR_144351.1:n.1253G>T
|
|
|
NM_001065.4:c.1024G>T
MANE Select
|
NP_001056.1:p.Glu342Ter
|
|
NM_001346091.2:c.700G>T
|
NP_001333020.1:p.Glu234Ter
|
|
NM_001346092.2:c.565G>T
|
NP_001333021.1:p.Glu189Ter
|
|
NR_144351.2:n.1212G>T
|
|
|