ENST00000697149.1:c.1696C>T
|
ENSP00000513138.1:n.1696C>T
|
|
ENST00000697150.1:c.1754C>T
|
ENSP00000513139.1:n.1754C>T
|
|
ENST00000697151.1:c.1687C>T
|
ENSP00000513140.1:n.1687C>T
|
|
ENST00000697164.1:c.1767C>T
|
ENSP00000513153.1:p.Ser589=
|
|
ENST00000697165.1:c.1554C>T
|
ENSP00000513154.1:p.Ser518=
|
|
ENST00000347310.10:c.1857C>T
MANE Select
|
ENSP00000321345.5:p.Ser619=
|
|
ENST00000637002.1:c.1248C>T
|
ENSP00000490340.1:p.Ser416=
|
|
ENST00000347310.9:c.1857C>T
|
ENSP00000321345.5:p.Ser619=
|
|
ENST00000395227.2:c.651C>T
|
ENSP00000378652.2:p.Ser217=
|
|
ENST00000425614.3:c.1092C>T
|
ENSP00000387640.2:p.Ser364=
|
|
ENST00000473881.2:c.*683C>T
|
ENSP00000486667.1:n.*683C>T
|
|
NM_144701.2:c.1857C>T
|
NP_653302.2:p.Ser619=
|
|
XM_005270516.2:c.1095C>T
|
XP_005270573.1:p.Ser365=
|
|
XM_011540789.1:c.1947C>T
|
XP_011539091.1:p.Ser649=
|
|
XM_011540790.1:c.1857C>T
|
XP_011539092.1:p.Ser619=
|
|
XM_011540791.1:c.1857C>T
|
XP_011539093.1:p.Ser619=
|
|
XM_011540790.3:c.1857C>T
|
XP_011539092.1:p.Ser619=
|
|
XM_011540791.3:c.1857C>T
|
XP_011539093.1:p.Ser619=
|
|
XR_001736993.1:n.1937C>T
|
|
|
NM_144701.3:c.1857C>T
MANE Select
|
NP_653302.2:p.Ser619=
|
|