ENST00000697149.1:c.1662T>G
|
ENSP00000513138.1:n.1662T>G
|
|
ENST00000697150.1:c.1720T>G
|
ENSP00000513139.1:n.1720T>G
|
|
ENST00000697151.1:c.1653T>G
|
ENSP00000513140.1:n.1653T>G
|
|
ENST00000697164.1:c.1733T>G
|
ENSP00000513153.1:p.Ile578Ser
|
|
ENST00000697165.1:c.1520T>G
|
ENSP00000513154.1:p.Ile507Ser
|
|
ENST00000347310.10:c.1823T>G
MANE Select
|
ENSP00000321345.5:p.Ile608Ser
|
|
ENST00000637002.1:c.1214T>G
|
ENSP00000490340.1:p.Ile405Ser
|
|
ENST00000347310.9:c.1823T>G
|
ENSP00000321345.5:p.Ile608Ser
|
|
ENST00000395227.2:c.617T>G
|
ENSP00000378652.2:p.Ile206Ser
|
|
ENST00000425614.3:c.1058T>G
|
ENSP00000387640.2:p.Ile353Ser
|
|
ENST00000473881.2:c.*649T>G
|
ENSP00000486667.1:n.*649T>G
|
|
NM_144701.2:c.1823T>G
|
NP_653302.2:p.Ile608Ser
|
|
XM_005270516.2:c.1061T>G
|
XP_005270573.1:p.Ile354Ser
|
|
XM_011540789.1:c.1913T>G
|
XP_011539091.1:p.Ile638Ser
|
|
XM_011540790.1:c.1823T>G
|
XP_011539092.1:p.Ile608Ser
|
|
XM_011540791.1:c.1823T>G
|
XP_011539093.1:p.Ile608Ser
|
|
XM_011540790.3:c.1823T>G
|
XP_011539092.1:p.Ile608Ser
|
|
XM_011540791.3:c.1823T>G
|
XP_011539093.1:p.Ile608Ser
|
|
XR_001736993.1:n.1903T>G
|
|
|
NM_144701.3:c.1823T>G
MANE Select
|
NP_653302.2:p.Ile608Ser
|
|