ENST00000334785.12:c.1470T>C
MANE Select
|
ENSP00000333938.7:p.His490=
|
|
ENST00000330010.12:c.1278T>C
|
ENSP00000327363.8:p.His426=
|
|
ENST00000334785.11:c.1470T>C
|
ENSP00000333938.7:p.His490=
|
|
ENST00000342754.5:c.1169T>C
|
|
|
ENST00000480732.2:n.1044T>C
|
|
|
NM_001172309.1:c.1278T>C
|
NP_001165780.1:p.His426=
|
|
NM_144573.3:c.1470T>C , LRG_442t1:c.1470T>C
|
NP_653174.3:p.His490=
|
|
XM_005271322.2:c.1470T>C
|
XP_005271379.1:p.His490=
|
|
XM_005271323.2:c.1428T>C
|
XP_005271380.1:p.His476=
|
|
XM_005271324.3:c.1278T>C
|
XP_005271381.1:p.His426=
|
|
XM_005271325.2:c.1251+2562T>C
|
XP_005271382.1:n.1251+2562T>C
|
|
XM_005271326.2:c.1236T>C
|
XP_005271383.1:p.His412=
|
|
XM_005271327.2:c.1053T>C
|
XP_005271384.1:p.His351=
|
|
XM_005271322.4:c.1470T>C
|
XP_005271379.1:p.His490=
|
|
XM_005271323.4:c.1428T>C
|
XP_005271380.1:p.His476=
|
|
XM_005271324.5:c.1278T>C
|
XP_005271381.1:p.His426=
|
|
XM_005271325.4:c.1251+2562T>C
|
XP_005271382.1:n.1251+2562T>C
|
|
XM_005271326.4:c.1236T>C
|
XP_005271383.1:p.His412=
|
|
XM_005271327.4:c.1053T>C
|
XP_005271384.1:p.His351=
|
|
NM_001172309.2:c.1278T>C
|
NP_001165780.1:p.His426=
|
|
NM_144573.4:c.1470T>C
MANE Select
|
NP_653174.3:p.His490=
|
|