ENST00000697149.1:c.1374C>G
|
ENSP00000513138.1:n.1374C>G
|
|
ENST00000697150.1:c.1432C>G
|
ENSP00000513139.1:n.1432C>G
|
|
ENST00000697151.1:c.1365C>G
|
ENSP00000513140.1:n.1365C>G
|
|
ENST00000697164.1:c.1445C>G
|
ENSP00000513153.1:p.Pro482Arg
|
|
ENST00000697165.1:c.1232C>G
|
ENSP00000513154.1:p.Pro411Arg
|
|
ENST00000347310.10:c.1535C>G
MANE Select
|
ENSP00000321345.5:p.Pro512Arg
|
|
ENST00000637002.1:c.926C>G
|
ENSP00000490340.1:p.Pro309Arg
|
|
ENST00000347310.9:c.1535C>G
|
ENSP00000321345.5:p.Pro512Arg
|
|
ENST00000395227.2:c.329C>G
|
ENSP00000378652.2:p.Pro110Arg
|
|
ENST00000425614.3:c.770C>G
|
ENSP00000387640.2:p.Pro257Arg
|
|
ENST00000473881.2:c.*361C>G
|
ENSP00000486667.1:n.*361C>G
|
|
NM_144701.2:c.1535C>G
|
NP_653302.2:p.Pro512Arg
|
|
XM_005270516.2:c.773C>G
|
XP_005270573.1:p.Pro258Arg
|
|
XM_011540789.1:c.1625C>G
|
XP_011539091.1:p.Pro542Arg
|
|
XM_011540790.1:c.1535C>G
|
XP_011539092.1:p.Pro512Arg
|
|
XM_011540791.1:c.1535C>G
|
XP_011539093.1:p.Pro512Arg
|
|
XM_011540790.3:c.1535C>G
|
XP_011539092.1:p.Pro512Arg
|
|
XM_011540791.3:c.1535C>G
|
XP_011539093.1:p.Pro512Arg
|
|
XR_001736993.1:n.1615C>G
|
|
|
NM_144701.3:c.1535C>G
MANE Select
|
NP_653302.2:p.Pro512Arg
|
|