ENST00000262367.10:c.4473A>T
MANE Select
|
ENSP00000262367.5:p.Gln1491His
|
|
ENST00000262367.9:c.4473A>T
|
ENSP00000262367.5:p.Gln1491His
|
|
ENST00000382070.7:c.4359A>T
|
ENSP00000371502.3:p.Gln1453His
|
|
ENST00000570939.2:c.3108A>T
|
ENSP00000461002.2:p.Gln1036His
|
|
ENST00000571763.5:n.263A>T
|
|
|
ENST00000574740.1:n.294A>T
|
|
|
ENST00000576720.1:n.3296A>T
|
|
|
NM_001079846.1:c.4359A>T
|
NP_001073315.1:p.Gln1453His
|
|
NM_004380.2:c.4473A>T
|
NP_004371.2:p.Gln1491His
|
|
XM_005255124.3:c.4428A>T
|
XP_005255181.1:p.Gln1476His
|
|
XM_005255125.3:c.4056A>T
|
XP_005255182.1:p.Gln1352His
|
|
XM_006720848.2:c.4212A>T
|
XP_006720911.1:p.Gln1404His
|
|
XM_011522380.1:c.4419A>T
|
XP_011520682.1:p.Gln1473His
|
|
XM_011522381.1:c.3720A>T
|
XP_011520683.1:p.Gln1240His
|
|
XM_005255124.4:c.4428A>T
|
XP_005255181.1:p.Gln1476His
|
|
XM_005255125.4:c.4056A>T
|
XP_005255182.1:p.Gln1352His
|
|
XM_006720848.3:c.4212A>T
|
XP_006720911.1:p.Gln1404His
|
|
XM_011522381.2:c.3720A>T
|
XP_011520683.1:p.Gln1240His
|
|
XM_017022944.1:c.4467A>T
|
XP_016878433.1:p.Gln1489His
|
|
NM_004380.3:c.4473A>T
MANE Select
|
NP_004371.2:p.Gln1491His
|
|