ENST00000334785.12:c.1477G>T
MANE Select
|
ENSP00000333938.7:p.Asp493Tyr
|
|
ENST00000330010.12:c.1285G>T
|
ENSP00000327363.8:p.Asp429Tyr
|
|
ENST00000334785.11:c.1477G>T
|
ENSP00000333938.7:p.Asp493Tyr
|
|
ENST00000342754.5:c.1176G>T
|
|
|
ENST00000470735.1:n.316G>T
|
|
|
ENST00000480732.2:n.1051G>T
|
|
|
NM_001172309.1:c.1285G>T
|
NP_001165780.1:p.Asp429Tyr
|
|
NM_144573.3:c.1477G>T , LRG_442t1:c.1477G>T
|
NP_653174.3:p.Asp493Tyr
|
|
XM_005271322.2:c.1477G>T
|
XP_005271379.1:p.Asp493Tyr
|
|
XM_005271323.2:c.1435G>T
|
XP_005271380.1:p.Asp479Tyr
|
|
XM_005271324.3:c.1285G>T
|
XP_005271381.1:p.Asp429Tyr
|
|
XM_005271325.2:c.1255G>T
|
XP_005271382.1:p.Asp419Tyr
|
|
XM_005271326.2:c.1243G>T
|
XP_005271383.1:p.Asp415Tyr
|
|
XM_005271327.2:c.1060G>T
|
XP_005271384.1:p.Asp354Tyr
|
|
XM_005271322.4:c.1477G>T
|
XP_005271379.1:p.Asp493Tyr
|
|
XM_005271323.4:c.1435G>T
|
XP_005271380.1:p.Asp479Tyr
|
|
XM_005271324.5:c.1285G>T
|
XP_005271381.1:p.Asp429Tyr
|
|
XM_005271325.4:c.1255G>T
|
XP_005271382.1:p.Asp419Tyr
|
|
XM_005271326.4:c.1243G>T
|
XP_005271383.1:p.Asp415Tyr
|
|
XM_005271327.4:c.1060G>T
|
XP_005271384.1:p.Asp354Tyr
|
|
NM_001172309.2:c.1285G>T
|
NP_001165780.1:p.Asp429Tyr
|
|
NM_144573.4:c.1477G>T
MANE Select
|
NP_653174.3:p.Asp493Tyr
|
|