ENST00000697149.1:c.1516T>G
|
ENSP00000513138.1:n.1516T>G
|
|
ENST00000697150.1:c.1574T>G
|
ENSP00000513139.1:n.1574T>G
|
|
ENST00000697151.1:c.1507T>G
|
ENSP00000513140.1:n.1507T>G
|
|
ENST00000697164.1:c.1587T>G
|
ENSP00000513153.1:p.Ser529Arg
|
|
ENST00000697165.1:c.1374T>G
|
ENSP00000513154.1:p.Ser458Arg
|
|
ENST00000347310.10:c.1677T>G
MANE Select
|
ENSP00000321345.5:p.Ser559Arg
|
|
ENST00000637002.1:c.1068T>G
|
ENSP00000490340.1:p.Ser356Arg
|
|
ENST00000347310.9:c.1677T>G
|
ENSP00000321345.5:p.Ser559Arg
|
|
ENST00000395227.2:c.471T>G
|
ENSP00000378652.2:p.Ser157Arg
|
|
ENST00000425614.3:c.912T>G
|
ENSP00000387640.2:p.Ser304Arg
|
|
ENST00000473881.2:c.*503T>G
|
ENSP00000486667.1:n.*503T>G
|
|
NM_144701.2:c.1677T>G
|
NP_653302.2:p.Ser559Arg
|
|
XM_005270516.2:c.915T>G
|
XP_005270573.1:p.Ser305Arg
|
|
XM_011540789.1:c.1767T>G
|
XP_011539091.1:p.Ser589Arg
|
|
XM_011540790.1:c.1677T>G
|
XP_011539092.1:p.Ser559Arg
|
|
XM_011540791.1:c.1677T>G
|
XP_011539093.1:p.Ser559Arg
|
|
XM_011540790.3:c.1677T>G
|
XP_011539092.1:p.Ser559Arg
|
|
XM_011540791.3:c.1677T>G
|
XP_011539093.1:p.Ser559Arg
|
|
XR_001736993.1:n.1757T>G
|
|
|
NM_144701.3:c.1677T>G
MANE Select
|
NP_653302.2:p.Ser559Arg
|
|