ENST00000697149.1:c.1592C>T
|
ENSP00000513138.1:n.1592C>T
|
|
ENST00000697150.1:c.1650C>T
|
ENSP00000513139.1:n.1650C>T
|
|
ENST00000697151.1:c.1583C>T
|
ENSP00000513140.1:n.1583C>T
|
|
ENST00000697164.1:c.1663C>T
|
ENSP00000513153.1:p.Pro555Ser
|
|
ENST00000697165.1:c.1450C>T
|
ENSP00000513154.1:p.Pro484Ser
|
|
ENST00000347310.10:c.1753C>T
MANE Select
|
ENSP00000321345.5:p.Pro585Ser
|
|
ENST00000637002.1:c.1144C>T
|
ENSP00000490340.1:p.Pro382Ser
|
|
ENST00000347310.9:c.1753C>T
|
ENSP00000321345.5:p.Pro585Ser
|
|
ENST00000395227.2:c.547C>T
|
ENSP00000378652.2:p.Pro183Ser
|
|
ENST00000425614.3:c.988C>T
|
ENSP00000387640.2:p.Pro330Ser
|
|
ENST00000473881.2:c.*579C>T
|
ENSP00000486667.1:n.*579C>T
|
|
NM_144701.2:c.1753C>T
|
NP_653302.2:p.Pro585Ser
|
|
XM_005270516.2:c.991C>T
|
XP_005270573.1:p.Pro331Ser
|
|
XM_011540789.1:c.1843C>T
|
XP_011539091.1:p.Pro615Ser
|
|
XM_011540790.1:c.1753C>T
|
XP_011539092.1:p.Pro585Ser
|
|
XM_011540791.1:c.1753C>T
|
XP_011539093.1:p.Pro585Ser
|
|
XM_011540790.3:c.1753C>T
|
XP_011539092.1:p.Pro585Ser
|
|
XM_011540791.3:c.1753C>T
|
XP_011539093.1:p.Pro585Ser
|
|
XR_001736993.1:n.1833C>T
|
|
|
NM_144701.3:c.1753C>T
MANE Select
|
NP_653302.2:p.Pro585Ser
|
|