ENST00000370192.8:c.181G>C
MANE Select
|
ENSP00000359211.3:p.Asp61His
|
|
ENST00000306031.5:c.181G>C
|
ENSP00000307107.5:p.Asp61His
|
|
ENST00000370192.7:c.181G>C
|
ENSP00000359211.3:p.Asp61His
|
|
NM_000110.3:c.181G>C , LRG_722t1:c.181G>C
|
NP_000101.2:p.Asp61His
|
|
NM_001160301.1:c.181G>C , LRG_722t2:c.181G>C
|
NP_001153773.1:p.Asp61His
|
|
XM_005270562.3:c.181G>C
|
XP_005270619.2:p.Asp61His
|
|
XM_006710397.2:c.181G>C
|
XP_006710460.1:p.Asp61His
|
|
XM_006710397.3:c.181G>C
|
XP_006710460.1:p.Asp61His
|
|
XM_017000507.1:c.70G>C
|
XP_016855996.1:p.Asp24His
|
|
XM_017000508.2:c.-530G>C
|
XP_016855997.1:n.-530G>C
|
|
XM_017000509.2:c.-428G>C
|
XP_016855998.1:n.-428G>C
|
|
XM_017000510.1:c.-428G>C
|
XP_016855999.1:n.-428G>C
|
|
XR_001737014.1:n.318G>C
|
|
|
NM_000110.4:c.181G>C
MANE Select
|
NP_000101.2:p.Asp61His
|
|