ENST00000697149.1:c.1454T>G
|
ENSP00000513138.1:n.1454T>G
|
|
ENST00000697150.1:c.1512T>G
|
ENSP00000513139.1:n.1512T>G
|
|
ENST00000697151.1:c.1445T>G
|
ENSP00000513140.1:n.1445T>G
|
|
ENST00000697164.1:c.1525T>G
|
ENSP00000513153.1:p.Ser509Ala
|
|
ENST00000697165.1:c.1312T>G
|
ENSP00000513154.1:p.Ser438Ala
|
|
ENST00000347310.10:c.1615T>G
MANE Select
|
ENSP00000321345.5:p.Ser539Ala
|
|
ENST00000637002.1:c.1006T>G
|
ENSP00000490340.1:p.Ser336Ala
|
|
ENST00000347310.9:c.1615T>G
|
ENSP00000321345.5:p.Ser539Ala
|
|
ENST00000395227.2:c.409T>G
|
ENSP00000378652.2:p.Ser137Ala
|
|
ENST00000425614.3:c.850T>G
|
ENSP00000387640.2:p.Ser284Ala
|
|
ENST00000473881.2:c.*441T>G
|
ENSP00000486667.1:n.*441T>G
|
|
NM_144701.2:c.1615T>G
|
NP_653302.2:p.Ser539Ala
|
|
XM_005270516.2:c.853T>G
|
XP_005270573.1:p.Ser285Ala
|
|
XM_011540789.1:c.1705T>G
|
XP_011539091.1:p.Ser569Ala
|
|
XM_011540790.1:c.1615T>G
|
XP_011539092.1:p.Ser539Ala
|
|
XM_011540791.1:c.1615T>G
|
XP_011539093.1:p.Ser539Ala
|
|
XM_011540790.3:c.1615T>G
|
XP_011539092.1:p.Ser539Ala
|
|
XM_011540791.3:c.1615T>G
|
XP_011539093.1:p.Ser539Ala
|
|
XR_001736993.1:n.1695T>G
|
|
|
NM_144701.3:c.1615T>G
MANE Select
|
NP_653302.2:p.Ser539Ala
|
|