|
ENST00000279227.10:c.1423G=
|
ENSP00000279227.5:p.Ala475=
|
|
|
ENST00000540554.2:n.2589G=
|
|
|
|
ENST00000541252.2:c.871G=
|
ENSP00000438885.2:p.Ala291=
|
|
|
ENST00000541326.6:n.832G=
|
|
|
|
ENST00000544997.6:c.1411G=
|
ENSP00000445778.2:p.Ala471=
|
|
|
ENST00000545896.2:c.100G=
|
ENSP00000440209.2:p.Ala34=
|
|
|
ENST00000546255.2:n.1715G=
|
|
|
|
ENST00000698845.1:c.*606G=
|
ENSP00000513981.1:n.*606G=
|
|
|
ENST00000698846.1:n.1657G=
|
|
|
|
ENST00000698847.1:c.*816G=
|
ENSP00000513982.1:n.*816G=
|
|
|
ENST00000698849.1:n.531G=
|
|
|
|
ENST00000698850.1:n.1179G=
|
|
|
|
ENST00000698852.1:c.1411G=
|
ENSP00000513984.1:p.Ala471=
|
|
|
ENST00000698853.1:c.*640G=
|
ENSP00000513985.1:n.*640G=
|
|
|
ENST00000698854.1:c.*741G=
|
ENSP00000513986.1:n.*741G=
|
|
|
ENST00000698855.1:n.3063G=
|
|
|
|
ENST00000698856.1:n.2757G=
|
|
|
|
ENST00000698859.1:n.1575G=
|
|
|
|
ENST00000698860.1:c.1423G=
|
ENSP00000513988.1:p.Ala475=
|
|
|
ENST00000698861.1:c.1411G=
|
ENSP00000513989.1:p.Ala471=
|
|
|
ENST00000698862.1:c.*707G=
|
ENSP00000513990.1:n.*707G=
|
|
|
ENST00000698863.1:c.1411G=
|
ENSP00000513991.1:p.Ala471=
|
|
|
ENST00000698864.1:n.1626G=
|
|
|
|
ENST00000698865.1:c.1432G=
|
ENSP00000513992.1:p.Ala478=
|
|
|
ENST00000698866.1:c.*925G=
|
ENSP00000513993.1:n.*925G=
|
|
|
ENST00000698867.1:n.5386G=
|
|
|
|
ENST00000698868.1:c.1276G=
|
ENSP00000513994.1:p.Ala426=
|
|
|
ENST00000698869.1:c.1311+209G=
|
ENSP00000513995.1:n.1311+209G=
|
|
|
ENST00000698870.1:c.1411G=
|
ENSP00000513996.1:p.Ala471=
|
|
|
ENST00000698871.1:n.1934G=
|
|
|
|
ENST00000698872.1:c.*200G=
|
ENSP00000513997.1:n.*200G=
|
|
|
ENST00000698873.1:c.*606G=
|
ENSP00000513998.1:n.*606G=
|
|
|
ENST00000698874.1:c.871G=
|
ENSP00000513999.1:p.Ala291=
|
|
|
ENST00000698875.1:n.1271G=
|
|
|
|
ENST00000698876.1:n.1459G=
|
|
|
|
ENST00000698877.1:n.979G=
|
|
|
|
ENST00000698878.1:c.1405G=
|
ENSP00000514000.1:p.Ala469=
|
|
|
ENST00000698880.1:c.1279G=
|
|
|
|
ENST00000345728.10:c.1411G=
MANE Select
|
ENSP00000339950.5:p.Ala471=
|
|
|
ENST00000279227.9:c.1423G=
|
ENSP00000279227.5:p.Ala475=
|
|
|
ENST00000345728.9:c.1411G=
|
ENSP00000339950.5:p.Ala471=
|
|
|
ENST00000541326.5:n.827G=
|
|
|
|
ENST00000545896.1:c.99G=
|
ENSP00000440209.1:p.Trp33=
|
|
|
NM_031471.5:c.1411G=
|
NP_113659.3:p.Ala471=
|
|
|
NM_178443.2:c.1423G= , LRG_180t1:c.1423G=
|
NP_848537.1:p.Ala475=
|
|
|
XM_011545294.1:c.1423G=
|
XP_011543596.1:p.Ala475=
|
|
|
XM_011545295.1:c.883G=
|
XP_011543597.1:p.Ala295=
|
|
|
XM_011545296.1:c.883G=
|
XP_011543598.1:p.Ala295=
|
|
|
XM_011545294.3:c.1423G=
|
XP_011543596.1:p.Ala475=
|
|
|
XM_011545295.2:c.883G=
|
XP_011543597.1:p.Ala295=
|
|
|
XM_017018398.2:c.1411G=
|
XP_016873887.1:p.Ala471=
|
|
|
XM_017018399.1:c.871G=
|
XP_016873888.1:p.Ala291=
|
|
|
NM_031471.6:c.1411G=
MANE Select
|
NP_113659.3:p.Ala471=
|
|
|
NM_001382361.1:c.1411G=
|
NP_001369290.1:p.Ala471=
|
|
|
NM_001382362.1:c.1423G=
|
NP_001369291.1:p.Ala475=
|
|
|
NM_001382363.1:c.871G=
|
NP_001369292.1:p.Ala291=
|
|
|
NM_001382364.1:c.883G=
|
NP_001369293.1:p.Ala295=
|
|
|
NM_001382448.1:c.1411G=
|
NP_001369377.1:p.Ala471=
|
|
|
NM_178443.3:c.1423G=
|
NP_848537.1:p.Ala475=
|
|
