ENST00000348974.5:c.1508C>T
|
ENSP00000330021.7:p.Ala503Val
|
|
ENST00000394236.9:c.1508C>T
MANE Select
|
ENSP00000377783.3:p.Ala503Val
|
|
ENST00000407433.6:c.1463C>T
|
ENSP00000385794.2:p.Ala488Val
|
|
ENST00000647936.1:c.1508C>T
|
ENSP00000496822.1:p.Ala503Val
|
|
ENST00000648381.1:n.1676C>T
|
|
|
ENST00000648853.1:c.1466C>T
|
ENSP00000497262.1:p.Ala489Val
|
|
ENST00000649103.1:c.1607C>T
|
ENSP00000497962.1:n.1607C>T
|
|
ENST00000649585.1:c.451C>T
|
ENSP00000498163.1:n.451C>T
|
|
ENST00000650591.1:c.1604C>T
|
ENSP00000497376.1:p.Ala535Val
|
|
ENST00000394236.7:c.1508C>T
|
ENSP00000377783.3:p.Ala503Val
|
|
ENST00000407433.5:c.1115C>T
|
ENSP00000385794.1:p.Ala372Val
|
|
NM_000313.3:c.1508C>T , LRG_572t1:c.1508C>T
|
NP_000304.2:p.Ala503Val
|
|
NM_001314077.1:c.1604C>T , LRG_572t2:c.1604C>T
|
NP_001301006.1:p.Ala535Val
|
|
NM_000313.4:c.1508C>T
MANE Select
|
NP_000304.2:p.Ala503Val
|
|
NM_001314077.2:c.1604C>T
|
NP_001301006.1:p.Ala535Val
|
|