ENST00000334785.12:c.1647A>T
MANE Select
|
ENSP00000333938.7:p.Ala549=
|
|
ENST00000330010.12:c.1455A>T
|
ENSP00000327363.8:p.Ala485=
|
|
ENST00000334785.11:c.1647A>T
|
ENSP00000333938.7:p.Ala549=
|
|
ENST00000342754.5:c.1346A>T
|
|
|
ENST00000470735.1:n.486A>T
|
|
|
ENST00000480732.2:n.1221A>T
|
|
|
NM_001172309.1:c.1455A>T
|
NP_001165780.1:p.Ala485=
|
|
NM_144573.3:c.1647A>T , LRG_442t1:c.1647A>T
|
NP_653174.3:p.Ala549=
|
|
XM_005271322.2:c.1647A>T
|
XP_005271379.1:p.Ala549=
|
|
XM_005271323.2:c.1605A>T
|
XP_005271380.1:p.Ala535=
|
|
XM_005271324.3:c.1455A>T
|
XP_005271381.1:p.Ala485=
|
|
XM_005271325.2:c.1425A>T
|
XP_005271382.1:p.Ala475=
|
|
XM_005271326.2:c.1413A>T
|
XP_005271383.1:p.Ala471=
|
|
XM_005271327.2:c.1230A>T
|
XP_005271384.1:p.Ala410=
|
|
XM_005271322.4:c.1647A>T
|
XP_005271379.1:p.Ala549=
|
|
XM_005271323.4:c.1605A>T
|
XP_005271380.1:p.Ala535=
|
|
XM_005271324.5:c.1455A>T
|
XP_005271381.1:p.Ala485=
|
|
XM_005271325.4:c.1425A>T
|
XP_005271382.1:p.Ala475=
|
|
XM_005271326.4:c.1413A>T
|
XP_005271383.1:p.Ala471=
|
|
XM_005271327.4:c.1230A>T
|
XP_005271384.1:p.Ala410=
|
|
NM_001172309.2:c.1455A>T
|
NP_001165780.1:p.Ala485=
|
|
NM_144573.4:c.1647A>T
MANE Select
|
NP_653174.3:p.Ala549=
|
|