|
ENST00000279227.10:c.1336G=
|
ENSP00000279227.5:p.Ala446=
|
|
|
ENST00000540554.2:n.2502G=
|
|
|
|
ENST00000541252.2:c.784G=
|
ENSP00000438885.2:p.Ala262=
|
|
|
ENST00000541326.6:n.745G=
|
|
|
|
ENST00000544997.6:c.1324G=
|
ENSP00000445778.2:p.Ala442=
|
|
|
ENST00000545896.2:c.13G=
|
ENSP00000440209.2:p.Ala5=
|
|
|
ENST00000546255.2:n.1628G=
|
|
|
|
ENST00000698845.1:c.*519G=
|
ENSP00000513981.1:n.*519G=
|
|
|
ENST00000698846.1:n.1570G=
|
|
|
|
ENST00000698847.1:c.*729G=
|
ENSP00000513982.1:n.*729G=
|
|
|
ENST00000698848.1:n.622G=
|
|
|
|
ENST00000698849.1:n.444G=
|
|
|
|
ENST00000698850.1:n.1092G=
|
|
|
|
ENST00000698852.1:c.1324G=
|
ENSP00000513984.1:p.Ala442=
|
|
|
ENST00000698853.1:c.*553G=
|
ENSP00000513985.1:n.*553G=
|
|
|
ENST00000698854.1:c.*654G=
|
ENSP00000513986.1:n.*654G=
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|
|
ENST00000698855.1:n.2976G=
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|
|
|
ENST00000698856.1:n.2670G=
|
|
|
|
ENST00000698859.1:n.1488G=
|
|
|
|
ENST00000698860.1:c.1336G=
|
ENSP00000513988.1:p.Ala446=
|
|
|
ENST00000698861.1:c.1324G=
|
ENSP00000513989.1:p.Ala442=
|
|
|
ENST00000698862.1:c.*620G=
|
ENSP00000513990.1:n.*620G=
|
|
|
ENST00000698863.1:c.1324G=
|
ENSP00000513991.1:p.Ala442=
|
|
|
ENST00000698864.1:n.1539G=
|
|
|
|
ENST00000698865.1:c.1345G=
|
ENSP00000513992.1:p.Ala449=
|
|
|
ENST00000698866.1:c.*838G=
|
ENSP00000513993.1:n.*838G=
|
|
|
ENST00000698867.1:n.5299G=
|
|
|
|
ENST00000698868.1:c.1189G=
|
ENSP00000513994.1:p.Ala397=
|
|
|
ENST00000698869.1:c.1311+122G=
|
ENSP00000513995.1:n.1311+122G=
|
|
|
ENST00000698870.1:c.1324G=
|
ENSP00000513996.1:p.Ala442=
|
|
|
ENST00000698871.1:n.1847G=
|
|
|
|
ENST00000698872.1:c.*113G=
|
ENSP00000513997.1:n.*113G=
|
|
|
ENST00000698873.1:c.*519G=
|
ENSP00000513998.1:n.*519G=
|
|
|
ENST00000698874.1:c.784G=
|
ENSP00000513999.1:p.Ala262=
|
|
|
ENST00000698875.1:n.1184G=
|
|
|
|
ENST00000698876.1:n.1372G=
|
|
|
|
ENST00000698877.1:n.892G=
|
|
|
|
ENST00000698878.1:c.1318G=
|
ENSP00000514000.1:p.Ala440=
|
|
|
ENST00000698880.1:c.1192G=
|
|
|
|
ENST00000345728.10:c.1324G=
MANE Select
|
ENSP00000339950.5:p.Ala442=
|
|
|
ENST00000279227.9:c.1336G=
|
ENSP00000279227.5:p.Ala446=
|
|
|
ENST00000345728.9:c.1324G=
|
ENSP00000339950.5:p.Ala442=
|
|
|
ENST00000540957.1:n.586G=
|
|
|
|
ENST00000541326.5:n.740G=
|
|
|
|
ENST00000545896.1:c.12G=
|
ENSP00000440209.1:p.Met4=
|
|
|
NM_031471.5:c.1324G=
|
NP_113659.3:p.Ala442=
|
|
|
NM_178443.2:c.1336G= , LRG_180t1:c.1336G=
|
NP_848537.1:p.Ala446=
|
|
|
XM_011545294.1:c.1336G=
|
XP_011543596.1:p.Ala446=
|
|
|
XM_011545295.1:c.796G=
|
XP_011543597.1:p.Ala266=
|
|
|
XM_011545296.1:c.796G=
|
XP_011543598.1:p.Ala266=
|
|
|
XM_011545294.3:c.1336G=
|
XP_011543596.1:p.Ala446=
|
|
|
XM_011545295.2:c.796G=
|
XP_011543597.1:p.Ala266=
|
|
|
XM_017018398.2:c.1324G=
|
XP_016873887.1:p.Ala442=
|
|
|
XM_017018399.1:c.784G=
|
XP_016873888.1:p.Ala262=
|
|
|
NM_031471.6:c.1324G=
MANE Select
|
NP_113659.3:p.Ala442=
|
|
|
NM_001382361.1:c.1324G=
|
NP_001369290.1:p.Ala442=
|
|
|
NM_001382362.1:c.1336G=
|
NP_001369291.1:p.Ala446=
|
|
|
NM_001382363.1:c.784G=
|
NP_001369292.1:p.Ala262=
|
|
|
NM_001382364.1:c.796G=
|
NP_001369293.1:p.Ala266=
|
|
|
NM_001382448.1:c.1324G=
|
NP_001369377.1:p.Ala442=
|
|
|
NM_178443.3:c.1336G=
|
NP_848537.1:p.Ala446=
|
|
