ENST00000697149.1:c.1653T>C
|
ENSP00000513138.1:n.1653T>C
|
|
ENST00000697150.1:c.1711T>C
|
ENSP00000513139.1:n.1711T>C
|
|
ENST00000697151.1:c.1644T>C
|
ENSP00000513140.1:n.1644T>C
|
|
ENST00000697164.1:c.1724T>C
|
ENSP00000513153.1:p.Leu575Ser
|
|
ENST00000697165.1:c.1511T>C
|
ENSP00000513154.1:p.Leu504Ser
|
|
ENST00000347310.10:c.1814T>C
MANE Select
|
ENSP00000321345.5:p.Leu605Ser
|
|
ENST00000637002.1:c.1205T>C
|
ENSP00000490340.1:p.Leu402Ser
|
|
ENST00000347310.9:c.1814T>C
|
ENSP00000321345.5:p.Leu605Ser
|
|
ENST00000395227.2:c.608T>C
|
ENSP00000378652.2:p.Leu203Ser
|
|
ENST00000425614.3:c.1049T>C
|
ENSP00000387640.2:p.Leu350Ser
|
|
ENST00000473881.2:c.*640T>C
|
ENSP00000486667.1:n.*640T>C
|
|
NM_144701.2:c.1814T>C
|
NP_653302.2:p.Leu605Ser
|
|
XM_005270516.2:c.1052T>C
|
XP_005270573.1:p.Leu351Ser
|
|
XM_011540789.1:c.1904T>C
|
XP_011539091.1:p.Leu635Ser
|
|
XM_011540790.1:c.1814T>C
|
XP_011539092.1:p.Leu605Ser
|
|
XM_011540791.1:c.1814T>C
|
XP_011539093.1:p.Leu605Ser
|
|
XM_011540790.3:c.1814T>C
|
XP_011539092.1:p.Leu605Ser
|
|
XM_011540791.3:c.1814T>C
|
XP_011539093.1:p.Leu605Ser
|
|
XR_001736993.1:n.1894T>C
|
|
|
NM_144701.3:c.1814T>C
MANE Select
|
NP_653302.2:p.Leu605Ser
|
|