ENST00000697149.1:c.1637A>T
|
ENSP00000513138.1:n.1637A>T
|
|
ENST00000697150.1:c.1695A>T
|
ENSP00000513139.1:n.1695A>T
|
|
ENST00000697151.1:c.1628A>T
|
ENSP00000513140.1:n.1628A>T
|
|
ENST00000697164.1:c.1708A>T
|
ENSP00000513153.1:p.Ile570Phe
|
|
ENST00000697165.1:c.1495A>T
|
ENSP00000513154.1:p.Ile499Phe
|
|
ENST00000347310.10:c.1798A>T
MANE Select
|
ENSP00000321345.5:p.Ile600Phe
|
|
ENST00000637002.1:c.1189A>T
|
ENSP00000490340.1:p.Ile397Phe
|
|
ENST00000347310.9:c.1798A>T
|
ENSP00000321345.5:p.Ile600Phe
|
|
ENST00000395227.2:c.592A>T
|
ENSP00000378652.2:p.Ile198Phe
|
|
ENST00000425614.3:c.1033A>T
|
ENSP00000387640.2:p.Ile345Phe
|
|
ENST00000473881.2:c.*624A>T
|
ENSP00000486667.1:n.*624A>T
|
|
NM_144701.2:c.1798A>T
|
NP_653302.2:p.Ile600Phe
|
|
XM_005270516.2:c.1036A>T
|
XP_005270573.1:p.Ile346Phe
|
|
XM_011540789.1:c.1888A>T
|
XP_011539091.1:p.Ile630Phe
|
|
XM_011540790.1:c.1798A>T
|
XP_011539092.1:p.Ile600Phe
|
|
XM_011540791.1:c.1798A>T
|
XP_011539093.1:p.Ile600Phe
|
|
XM_011540790.3:c.1798A>T
|
XP_011539092.1:p.Ile600Phe
|
|
XM_011540791.3:c.1798A>T
|
XP_011539093.1:p.Ile600Phe
|
|
XR_001736993.1:n.1878A>T
|
|
|
NM_144701.3:c.1798A>T
MANE Select
|
NP_653302.2:p.Ile600Phe
|
|