ENST00000348974.5:c.2006T>G
|
ENSP00000330021.7:p.Val669Gly
|
|
ENST00000394236.9:c.2006T>G
MANE Select
|
ENSP00000377783.3:p.Val669Gly
|
|
ENST00000407433.6:c.1961T>G
|
ENSP00000385794.2:p.Val654Gly
|
|
ENST00000647936.1:c.*109T>G
|
ENSP00000496822.1:n.*109T>G
|
|
ENST00000648381.1:n.2174T>G
|
|
|
ENST00000648853.1:c.1964T>G
|
ENSP00000497262.1:p.Val655Gly
|
|
ENST00000650591.1:c.2102T>G
|
ENSP00000497376.1:p.Val701Gly
|
|
ENST00000394236.7:c.2006T>G
|
ENSP00000377783.3:p.Val669Gly
|
|
ENST00000407433.5:c.1613T>G
|
ENSP00000385794.1:p.Val538Gly
|
|
NM_000313.3:c.2006T>G , LRG_572t1:c.2006T>G
|
NP_000304.2:p.Val669Gly
|
|
NM_001314077.1:c.2102T>G , LRG_572t2:c.2102T>G
|
NP_001301006.1:p.Val701Gly
|
|
NM_000313.4:c.2006T>G
MANE Select
|
NP_000304.2:p.Val669Gly
|
|
NM_001314077.2:c.2102T>G
|
NP_001301006.1:p.Val701Gly
|
|