ENST00000697149.1:c.1478G>A
|
ENSP00000513138.1:n.1478G>A
|
|
ENST00000697150.1:c.1536G>A
|
ENSP00000513139.1:n.1536G>A
|
|
ENST00000697151.1:c.1469G>A
|
ENSP00000513140.1:n.1469G>A
|
|
ENST00000697164.1:c.1549G>A
|
ENSP00000513153.1:p.Gly517Arg
|
|
ENST00000697165.1:c.1336G>A
|
ENSP00000513154.1:p.Gly446Arg
|
|
ENST00000347310.10:c.1639G>A
MANE Select
|
ENSP00000321345.5:p.Gly547Arg
|
|
ENST00000637002.1:c.1030G>A
|
ENSP00000490340.1:p.Gly344Arg
|
|
ENST00000347310.9:c.1639G>A
|
ENSP00000321345.5:p.Gly547Arg
|
|
ENST00000395227.2:c.433G>A
|
ENSP00000378652.2:p.Gly145Arg
|
|
ENST00000425614.3:c.874G>A
|
ENSP00000387640.2:p.Gly292Arg
|
|
ENST00000473881.2:c.*465G>A
|
ENSP00000486667.1:n.*465G>A
|
|
NM_144701.2:c.1639G>A
|
NP_653302.2:p.Gly547Arg
|
|
XM_005270516.2:c.877G>A
|
XP_005270573.1:p.Gly293Arg
|
|
XM_011540789.1:c.1729G>A
|
XP_011539091.1:p.Gly577Arg
|
|
XM_011540790.1:c.1639G>A
|
XP_011539092.1:p.Gly547Arg
|
|
XM_011540791.1:c.1639G>A
|
XP_011539093.1:p.Gly547Arg
|
|
XM_011540790.3:c.1639G>A
|
XP_011539092.1:p.Gly547Arg
|
|
XM_011540791.3:c.1639G>A
|
XP_011539093.1:p.Gly547Arg
|
|
XR_001736993.1:n.1719G>A
|
|
|
NM_144701.3:c.1639G>A
MANE Select
|
NP_653302.2:p.Gly547Arg
|
|