ENST00000697149.1:c.1470T>C
|
ENSP00000513138.1:n.1470T>C
|
|
ENST00000697150.1:c.1528T>C
|
ENSP00000513139.1:n.1528T>C
|
|
ENST00000697151.1:c.1461T>C
|
ENSP00000513140.1:n.1461T>C
|
|
ENST00000697164.1:c.1541T>C
|
ENSP00000513153.1:p.Ile514Thr
|
|
ENST00000697165.1:c.1328T>C
|
ENSP00000513154.1:p.Ile443Thr
|
|
ENST00000347310.10:c.1631T>C
MANE Select
|
ENSP00000321345.5:p.Ile544Thr
|
|
ENST00000637002.1:c.1022T>C
|
ENSP00000490340.1:p.Ile341Thr
|
|
ENST00000347310.9:c.1631T>C
|
ENSP00000321345.5:p.Ile544Thr
|
|
ENST00000395227.2:c.425T>C
|
ENSP00000378652.2:p.Ile142Thr
|
|
ENST00000425614.3:c.866T>C
|
ENSP00000387640.2:p.Ile289Thr
|
|
ENST00000473881.2:c.*457T>C
|
ENSP00000486667.1:n.*457T>C
|
|
NM_144701.2:c.1631T>C
|
NP_653302.2:p.Ile544Thr
|
|
XM_005270516.2:c.869T>C
|
XP_005270573.1:p.Ile290Thr
|
|
XM_011540789.1:c.1721T>C
|
XP_011539091.1:p.Ile574Thr
|
|
XM_011540790.1:c.1631T>C
|
XP_011539092.1:p.Ile544Thr
|
|
XM_011540791.1:c.1631T>C
|
XP_011539093.1:p.Ile544Thr
|
|
XM_011540790.3:c.1631T>C
|
XP_011539092.1:p.Ile544Thr
|
|
XM_011540791.3:c.1631T>C
|
XP_011539093.1:p.Ile544Thr
|
|
XR_001736993.1:n.1711T>C
|
|
|
NM_144701.3:c.1631T>C
MANE Select
|
NP_653302.2:p.Ile544Thr
|
|