ENST00000279227.10:c.1708A>G
|
ENSP00000279227.5:p.Ile570Val
|
|
ENST00000540554.2:n.3220A>G
|
|
|
ENST00000541252.2:c.1156A>G
|
ENSP00000438885.2:p.Ile386Val
|
|
ENST00000544997.6:c.1696A>G
|
ENSP00000445778.2:p.Ile566Val
|
|
ENST00000545896.2:c.260A>G
|
ENSP00000440209.2:p.Asp87Gly
|
|
ENST00000546255.2:n.2000A>G
|
|
|
ENST00000698845.1:c.*891A>G
|
ENSP00000513981.1:n.*891A>G
|
|
ENST00000698846.1:n.1942A>G
|
|
|
ENST00000698847.1:c.*1101A>G
|
ENSP00000513982.1:n.*1101A>G
|
|
ENST00000698850.1:n.3717A>G
|
|
|
ENST00000698852.1:c.1696A>G
|
ENSP00000513984.1:p.Ile566Val
|
|
ENST00000698853.1:c.*925A>G
|
ENSP00000513985.1:n.*925A>G
|
|
ENST00000698854.1:c.*1026A>G
|
ENSP00000513986.1:n.*1026A>G
|
|
ENST00000698855.1:n.3348A>G
|
|
|
ENST00000698856.1:n.3042A>G
|
|
|
ENST00000698859.1:n.2206A>G
|
|
|
ENST00000698860.1:c.1708A>G
|
ENSP00000513988.1:p.Ile570Val
|
|
ENST00000698861.1:c.1696A>G
|
ENSP00000513989.1:p.Ile566Val
|
|
ENST00000698862.1:c.*992A>G
|
ENSP00000513990.1:n.*992A>G
|
|
ENST00000698863.1:c.1696A>G
|
ENSP00000513991.1:p.Ile566Val
|
|
ENST00000698864.1:n.2257A>G
|
|
|
ENST00000698865.1:c.1717A>G
|
ENSP00000513992.1:p.Ile573Val
|
|
ENST00000698866.1:c.*1484A>G
|
ENSP00000513993.1:n.*1484A>G
|
|
ENST00000698867.1:n.5671A>G
|
|
|
ENST00000698868.1:c.1561A>G
|
ENSP00000513994.1:p.Ile521Val
|
|
ENST00000698869.1:c.1462A>G
|
ENSP00000513995.1:p.Ile488Val
|
|
ENST00000698870.1:c.1696A>G
|
ENSP00000513996.1:p.Ile566Val
|
|
ENST00000698871.1:n.2219A>G
|
|
|
ENST00000698872.1:c.*485A>G
|
ENSP00000513997.1:n.*485A>G
|
|
ENST00000698873.1:c.*891A>G
|
ENSP00000513998.1:n.*891A>G
|
|
ENST00000698874.1:c.1156A>G
|
ENSP00000513999.1:p.Ile386Val
|
|
ENST00000698875.1:n.1556A>G
|
|
|
ENST00000698876.1:n.1744A>G
|
|
|
ENST00000698877.1:n.1264A>G
|
|
|
ENST00000698878.1:c.1690A>G
|
ENSP00000514000.1:p.Ile564Val
|
|
ENST00000698880.1:c.1564A>G
|
|
|
ENST00000345728.10:c.1696A>G
MANE Select
|
ENSP00000339950.5:p.Ile566Val
|
|
ENST00000279227.9:c.1708A>G
|
ENSP00000279227.5:p.Ile570Val
|
|
ENST00000345728.9:c.1696A>G
|
ENSP00000339950.5:p.Ile566Val
|
|
ENST00000540554.1:n.332A>G
|
|
|
ENST00000545896.1:c.259A>G
|
ENSP00000440209.1:p.Ile87Val
|
|
NM_031471.5:c.1696A>G
|
NP_113659.3:p.Ile566Val
|
|
NM_178443.2:c.1708A>G , LRG_180t1:c.1708A>G
|
NP_848537.1:p.Ile570Val
|
|
XM_011545294.1:c.1708A>G
|
XP_011543596.1:p.Ile570Val
|
|
XM_011545295.1:c.1168A>G
|
XP_011543597.1:p.Ile390Val
|
|
XM_011545296.1:c.1168A>G
|
XP_011543598.1:p.Ile390Val
|
|
XM_011545294.3:c.1708A>G
|
XP_011543596.1:p.Ile570Val
|
|
XM_011545295.2:c.1168A>G
|
XP_011543597.1:p.Ile390Val
|
|
XM_017018398.2:c.1696A>G
|
XP_016873887.1:p.Ile566Val
|
|
XM_017018399.1:c.1156A>G
|
XP_016873888.1:p.Ile386Val
|
|
NM_031471.6:c.1696A>G
MANE Select
|
NP_113659.3:p.Ile566Val
|
|
NM_001382361.1:c.1696A>G
|
NP_001369290.1:p.Ile566Val
|
|
NM_001382362.1:c.1708A>G
|
NP_001369291.1:p.Ile570Val
|
|
NM_001382363.1:c.1156A>G
|
NP_001369292.1:p.Ile386Val
|
|
NM_001382364.1:c.1168A>G
|
NP_001369293.1:p.Ile390Val
|
|
NM_001382448.1:c.1696A>G
|
NP_001369377.1:p.Ile566Val
|
|
NM_178443.3:c.1708A>G
|
NP_848537.1:p.Ile570Val
|
|