ENST00000372517.8:c.387A>T
MANE Select
|
ENSP00000361595.2:p.Gln129His
|
|
ENST00000487556.6:n.452-3969A>T
|
|
|
ENST00000642150.1:n.574A>T
|
|
|
ENST00000647120.1:n.248-3969A>T
|
|
|
ENST00000328249.3:c.117A>T
|
ENSP00000332439.3:p.Gln39His
|
|
ENST00000372514.7:c.387A>T
|
ENSP00000361592.3:p.Gln129His
|
|
ENST00000372517.6:c.387A>T
|
ENSP00000361595.2:p.Gln129His
|
|
ENST00000487556.5:n.247-3969A>T
|
|
|
NM_001017922.1:c.387A>T
|
NP_001017922.1:p.Gln129His
|
|
NM_018538.3:c.387A>T
|
NP_061008.2:p.Gln129His
|
|
XM_006710313.2:c.387A>T
|
XP_006710376.1:p.Gln129His
|
|
XM_011540570.1:c.387A>T
|
XP_011538872.1:p.Gln129His
|
|
XM_011540571.1:c.387A>T
|
XP_011538873.1:p.Gln129His
|
|
XM_006710313.4:c.387A>T
|
XP_006710376.1:p.Gln129His
|
|
XM_011540570.3:c.387A>T
|
XP_011538872.1:p.Gln129His
|
|
XM_011540571.3:c.387A>T
|
XP_011538873.1:p.Gln129His
|
|
NM_001017922.2:c.387A>T
MANE Select
|
NP_001017922.1:p.Gln129His
|
|
NM_018538.4:c.387A>T
|
NP_061008.2:p.Gln129His
|
|