ENST00000279227.10:c.1744G>T
|
ENSP00000279227.5:p.Asp582Tyr
|
|
ENST00000540554.2:n.3256G>T
|
|
|
ENST00000541252.2:c.1192G>T
|
ENSP00000438885.2:p.Asp398Tyr
|
|
ENST00000544997.6:c.1732G>T
|
ENSP00000445778.2:p.Asp578Tyr
|
|
ENST00000545896.2:c.296G>T
|
ENSP00000440209.2:p.Arg99Leu
|
|
ENST00000546255.2:n.2036G>T
|
|
|
ENST00000698845.1:c.*927G>T
|
ENSP00000513981.1:n.*927G>T
|
|
ENST00000698846.1:n.1978G>T
|
|
|
ENST00000698847.1:c.*1137G>T
|
ENSP00000513982.1:n.*1137G>T
|
|
ENST00000698850.1:n.3753G>T
|
|
|
ENST00000698852.1:c.1732G>T
|
ENSP00000513984.1:p.Asp578Tyr
|
|
ENST00000698853.1:c.*961G>T
|
ENSP00000513985.1:n.*961G>T
|
|
ENST00000698854.1:c.*1062G>T
|
ENSP00000513986.1:n.*1062G>T
|
|
ENST00000698855.1:n.3384G>T
|
|
|
ENST00000698856.1:n.3078G>T
|
|
|
ENST00000698859.1:n.2242G>T
|
|
|
ENST00000698860.1:c.1744G>T
|
ENSP00000513988.1:p.Asp582Tyr
|
|
ENST00000698861.1:c.1732G>T
|
ENSP00000513989.1:p.Asp578Tyr
|
|
ENST00000698862.1:c.*1028G>T
|
ENSP00000513990.1:n.*1028G>T
|
|
ENST00000698863.1:c.1732G>T
|
ENSP00000513991.1:p.Asp578Tyr
|
|
ENST00000698864.1:n.2293G>T
|
|
|
ENST00000698865.1:c.1753G>T
|
ENSP00000513992.1:p.Asp585Tyr
|
|
ENST00000698866.1:c.*1520G>T
|
ENSP00000513993.1:n.*1520G>T
|
|
ENST00000698867.1:n.5707G>T
|
|
|
ENST00000698868.1:c.1597G>T
|
ENSP00000513994.1:p.Asp533Tyr
|
|
ENST00000698869.1:c.1498G>T
|
ENSP00000513995.1:p.Asp500Tyr
|
|
ENST00000698870.1:c.1732G>T
|
ENSP00000513996.1:p.Asp578Tyr
|
|
ENST00000698871.1:n.2255G>T
|
|
|
ENST00000698872.1:c.*521G>T
|
ENSP00000513997.1:n.*521G>T
|
|
ENST00000698873.1:c.*927G>T
|
ENSP00000513998.1:n.*927G>T
|
|
ENST00000698874.1:c.1192G>T
|
ENSP00000513999.1:p.Asp398Tyr
|
|
ENST00000698875.1:n.1592G>T
|
|
|
ENST00000698876.1:n.1780G>T
|
|
|
ENST00000698877.1:n.1300G>T
|
|
|
ENST00000698878.1:c.1726G>T
|
ENSP00000514000.1:p.Asp576Tyr
|
|
ENST00000698880.1:c.1600G>T
|
|
|
ENST00000345728.10:c.1732G>T
MANE Select
|
ENSP00000339950.5:p.Asp578Tyr
|
|
ENST00000279227.9:c.1744G>T
|
ENSP00000279227.5:p.Asp582Tyr
|
|
ENST00000345728.9:c.1732G>T
|
ENSP00000339950.5:p.Asp578Tyr
|
|
ENST00000540554.1:n.368G>T
|
|
|
ENST00000545896.1:c.295G>T
|
ENSP00000440209.1:p.Asp99Tyr
|
|
NM_031471.5:c.1732G>T
|
NP_113659.3:p.Asp578Tyr
|
|
NM_178443.2:c.1744G>T , LRG_180t1:c.1744G>T
|
NP_848537.1:p.Asp582Tyr
|
|
XM_011545294.1:c.1744G>T
|
XP_011543596.1:p.Asp582Tyr
|
|
XM_011545295.1:c.1204G>T
|
XP_011543597.1:p.Asp402Tyr
|
|
XM_011545296.1:c.1204G>T
|
XP_011543598.1:p.Asp402Tyr
|
|
XM_011545294.3:c.1744G>T
|
XP_011543596.1:p.Asp582Tyr
|
|
XM_011545295.2:c.1204G>T
|
XP_011543597.1:p.Asp402Tyr
|
|
XM_017018398.2:c.1732G>T
|
XP_016873887.1:p.Asp578Tyr
|
|
XM_017018399.1:c.1192G>T
|
XP_016873888.1:p.Asp398Tyr
|
|
NM_031471.6:c.1732G>T
MANE Select
|
NP_113659.3:p.Asp578Tyr
|
|
NM_001382361.1:c.1732G>T
|
NP_001369290.1:p.Asp578Tyr
|
|
NM_001382362.1:c.1744G>T
|
NP_001369291.1:p.Asp582Tyr
|
|
NM_001382363.1:c.1192G>T
|
NP_001369292.1:p.Asp398Tyr
|
|
NM_001382364.1:c.1204G>T
|
NP_001369293.1:p.Asp402Tyr
|
|
NM_001382448.1:c.1732G>T
|
NP_001369377.1:p.Asp578Tyr
|
|
NM_178443.3:c.1744G>T
|
NP_848537.1:p.Asp582Tyr
|
|