|
ENST00000279227.10:c.1484A=
|
ENSP00000279227.5:p.Asp495=
|
|
|
ENST00000540554.2:n.2650A=
|
|
|
|
ENST00000541252.2:c.932A=
|
ENSP00000438885.2:p.Asp311=
|
|
|
ENST00000541326.6:n.893A=
|
|
|
|
ENST00000544997.6:c.1472A=
|
ENSP00000445778.2:p.Asp491=
|
|
|
ENST00000545896.2:c.161A=
|
ENSP00000440209.2:p.Asp54=
|
|
|
ENST00000546255.2:n.1776A=
|
|
|
|
ENST00000698845.1:c.*667A=
|
ENSP00000513981.1:n.*667A=
|
|
|
ENST00000698846.1:n.1718A=
|
|
|
|
ENST00000698847.1:c.*877A=
|
ENSP00000513982.1:n.*877A=
|
|
|
ENST00000698849.1:n.592A=
|
|
|
|
ENST00000698850.1:n.1240A=
|
|
|
|
ENST00000698852.1:c.1472A=
|
ENSP00000513984.1:p.Asp491=
|
|
|
ENST00000698853.1:c.*701A=
|
ENSP00000513985.1:n.*701A=
|
|
|
ENST00000698854.1:c.*802A=
|
ENSP00000513986.1:n.*802A=
|
|
|
ENST00000698855.1:n.3124A=
|
|
|
|
ENST00000698856.1:n.2818A=
|
|
|
|
ENST00000698859.1:n.1636A=
|
|
|
|
ENST00000698860.1:c.1484A=
|
ENSP00000513988.1:p.Asp495=
|
|
|
ENST00000698861.1:c.1472A=
|
ENSP00000513989.1:p.Asp491=
|
|
|
ENST00000698862.1:c.*768A=
|
ENSP00000513990.1:n.*768A=
|
|
|
ENST00000698863.1:c.1472A=
|
ENSP00000513991.1:p.Asp491=
|
|
|
ENST00000698864.1:n.1687A=
|
|
|
|
ENST00000698865.1:c.1493A=
|
ENSP00000513992.1:p.Asp498=
|
|
|
ENST00000698866.1:c.*986A=
|
ENSP00000513993.1:n.*986A=
|
|
|
ENST00000698867.1:n.5447A=
|
|
|
|
ENST00000698868.1:c.1337A=
|
ENSP00000513994.1:p.Asp446=
|
|
|
ENST00000698869.1:c.1311+270A=
|
ENSP00000513995.1:n.1311+270A=
|
|
|
ENST00000698870.1:c.1472A=
|
ENSP00000513996.1:p.Asp491=
|
|
|
ENST00000698871.1:n.1995A=
|
|
|
|
ENST00000698872.1:c.*261A=
|
ENSP00000513997.1:n.*261A=
|
|
|
ENST00000698873.1:c.*667A=
|
ENSP00000513998.1:n.*667A=
|
|
|
ENST00000698874.1:c.932A=
|
ENSP00000513999.1:p.Asp311=
|
|
|
ENST00000698875.1:n.1332A=
|
|
|
|
ENST00000698876.1:n.1520A=
|
|
|
|
ENST00000698877.1:n.1040A=
|
|
|
|
ENST00000698878.1:c.1466A=
|
ENSP00000514000.1:p.Asp489=
|
|
|
ENST00000698880.1:c.1340A=
|
|
|
|
ENST00000345728.10:c.1472A=
MANE Select
|
ENSP00000339950.5:p.Asp491=
|
|
|
ENST00000279227.9:c.1484A=
|
ENSP00000279227.5:p.Asp495=
|
|
|
ENST00000345728.9:c.1472A=
|
ENSP00000339950.5:p.Asp491=
|
|
|
ENST00000541326.5:n.888A=
|
|
|
|
ENST00000545896.1:c.160A=
|
ENSP00000440209.1:p.Met54=
|
|
|
NM_031471.5:c.1472A=
|
NP_113659.3:p.Asp491=
|
|
|
NM_178443.2:c.1484A= , LRG_180t1:c.1484A=
|
NP_848537.1:p.Asp495=
|
|
|
XM_011545294.1:c.1484A=
|
XP_011543596.1:p.Asp495=
|
|
|
XM_011545295.1:c.944A=
|
XP_011543597.1:p.Asp315=
|
|
|
XM_011545296.1:c.944A=
|
XP_011543598.1:p.Asp315=
|
|
|
XM_011545294.3:c.1484A=
|
XP_011543596.1:p.Asp495=
|
|
|
XM_011545295.2:c.944A=
|
XP_011543597.1:p.Asp315=
|
|
|
XM_017018398.2:c.1472A=
|
XP_016873887.1:p.Asp491=
|
|
|
XM_017018399.1:c.932A=
|
XP_016873888.1:p.Asp311=
|
|
|
NM_031471.6:c.1472A=
MANE Select
|
NP_113659.3:p.Asp491=
|
|
|
NM_001382361.1:c.1472A=
|
NP_001369290.1:p.Asp491=
|
|
|
NM_001382362.1:c.1484A=
|
NP_001369291.1:p.Asp495=
|
|
|
NM_001382363.1:c.932A=
|
NP_001369292.1:p.Asp311=
|
|
|
NM_001382364.1:c.944A=
|
NP_001369293.1:p.Asp315=
|
|
|
NM_001382448.1:c.1472A=
|
NP_001369377.1:p.Asp491=
|
|
|
NM_178443.3:c.1484A=
|
NP_848537.1:p.Asp495=
|
|
