ENST00000697149.1:c.1395G>C
|
ENSP00000513138.1:n.1395G>C
|
|
ENST00000697150.1:c.1453G>C
|
ENSP00000513139.1:n.1453G>C
|
|
ENST00000697151.1:c.1386G>C
|
ENSP00000513140.1:n.1386G>C
|
|
ENST00000697164.1:c.1466G>C
|
ENSP00000513153.1:p.Gly489Ala
|
|
ENST00000697165.1:c.1253G>C
|
ENSP00000513154.1:p.Gly418Ala
|
|
ENST00000347310.10:c.1556G>C
MANE Select
|
ENSP00000321345.5:p.Gly519Ala
|
|
ENST00000637002.1:c.947G>C
|
ENSP00000490340.1:p.Gly316Ala
|
|
ENST00000347310.9:c.1556G>C
|
ENSP00000321345.5:p.Gly519Ala
|
|
ENST00000395227.2:c.350G>C
|
ENSP00000378652.2:p.Gly117Ala
|
|
ENST00000425614.3:c.791G>C
|
ENSP00000387640.2:p.Gly264Ala
|
|
ENST00000473881.2:c.*382G>C
|
ENSP00000486667.1:n.*382G>C
|
|
NM_144701.2:c.1556G>C
|
NP_653302.2:p.Gly519Ala
|
|
XM_005270516.2:c.794G>C
|
XP_005270573.1:p.Gly265Ala
|
|
XM_011540789.1:c.1646G>C
|
XP_011539091.1:p.Gly549Ala
|
|
XM_011540790.1:c.1556G>C
|
XP_011539092.1:p.Gly519Ala
|
|
XM_011540791.1:c.1556G>C
|
XP_011539093.1:p.Gly519Ala
|
|
XM_011540790.3:c.1556G>C
|
XP_011539092.1:p.Gly519Ala
|
|
XM_011540791.3:c.1556G>C
|
XP_011539093.1:p.Gly519Ala
|
|
XR_001736993.1:n.1636G>C
|
|
|
NM_144701.3:c.1556G>C
MANE Select
|
NP_653302.2:p.Gly519Ala
|
|