|
ENST00000279227.10:c.1750G=
|
ENSP00000279227.5:p.Ala584=
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|
|
ENST00000540554.2:n.3262G=
|
|
|
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ENST00000541252.2:c.1198G=
|
ENSP00000438885.2:p.Ala400=
|
|
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ENST00000544997.6:c.1738G=
|
ENSP00000445778.2:p.Ala580=
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|
|
ENST00000545896.2:c.302G=
|
ENSP00000440209.2:p.Gly101=
|
|
|
ENST00000546255.2:n.2042G=
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|
|
|
ENST00000698845.1:c.*933G=
|
ENSP00000513981.1:n.*933G=
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|
|
ENST00000698846.1:n.1984G=
|
|
|
|
ENST00000698847.1:c.*1143G=
|
ENSP00000513982.1:n.*1143G=
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|
|
ENST00000698850.1:n.3759G=
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|
|
|
ENST00000698852.1:c.1738G=
|
ENSP00000513984.1:p.Ala580=
|
|
|
ENST00000698853.1:c.*967G=
|
ENSP00000513985.1:n.*967G=
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|
|
ENST00000698854.1:c.*1068G=
|
ENSP00000513986.1:n.*1068G=
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|
|
ENST00000698855.1:n.3390G=
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|
|
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ENST00000698856.1:n.3084G=
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|
|
|
ENST00000698859.1:n.2248G=
|
|
|
|
ENST00000698860.1:c.1750G=
|
ENSP00000513988.1:p.Ala584=
|
|
|
ENST00000698861.1:c.1738G=
|
ENSP00000513989.1:p.Ala580=
|
|
|
ENST00000698862.1:c.*1034G=
|
ENSP00000513990.1:n.*1034G=
|
|
|
ENST00000698863.1:c.1738G=
|
ENSP00000513991.1:p.Ala580=
|
|
|
ENST00000698864.1:n.2299G=
|
|
|
|
ENST00000698865.1:c.1759G=
|
ENSP00000513992.1:p.Ala587=
|
|
|
ENST00000698866.1:c.*1526G=
|
ENSP00000513993.1:n.*1526G=
|
|
|
ENST00000698867.1:n.5713G=
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|
|
|
ENST00000698868.1:c.1603G=
|
ENSP00000513994.1:p.Ala535=
|
|
|
ENST00000698869.1:c.1504G=
|
ENSP00000513995.1:p.Ala502=
|
|
|
ENST00000698870.1:c.1738G=
|
ENSP00000513996.1:p.Ala580=
|
|
|
ENST00000698871.1:n.2261G=
|
|
|
|
ENST00000698872.1:c.*527G=
|
ENSP00000513997.1:n.*527G=
|
|
|
ENST00000698873.1:c.*933G=
|
ENSP00000513998.1:n.*933G=
|
|
|
ENST00000698874.1:c.1198G=
|
ENSP00000513999.1:p.Ala400=
|
|
|
ENST00000698875.1:n.1598G=
|
|
|
|
ENST00000698876.1:n.1786G=
|
|
|
|
ENST00000698877.1:n.1306G=
|
|
|
|
ENST00000698878.1:c.1732G=
|
ENSP00000514000.1:p.Ala578=
|
|
|
ENST00000698880.1:c.1606G=
|
|
|
|
ENST00000345728.10:c.1738G=
MANE Select
|
ENSP00000339950.5:p.Ala580=
|
|
|
ENST00000279227.9:c.1750G=
|
ENSP00000279227.5:p.Ala584=
|
|
|
ENST00000345728.9:c.1738G=
|
ENSP00000339950.5:p.Ala580=
|
|
|
ENST00000540554.1:n.374G=
|
|
|
|
ENST00000545896.1:c.301G=
|
ENSP00000440209.1:p.Ala101=
|
|
|
NM_031471.5:c.1738G=
|
NP_113659.3:p.Ala580=
|
|
|
NM_178443.2:c.1750G= , LRG_180t1:c.1750G=
|
NP_848537.1:p.Ala584=
|
|
|
XM_011545294.1:c.1750G=
|
XP_011543596.1:p.Ala584=
|
|
|
XM_011545295.1:c.1210G=
|
XP_011543597.1:p.Ala404=
|
|
|
XM_011545296.1:c.1210G=
|
XP_011543598.1:p.Ala404=
|
|
|
XM_011545294.3:c.1750G=
|
XP_011543596.1:p.Ala584=
|
|
|
XM_011545295.2:c.1210G=
|
XP_011543597.1:p.Ala404=
|
|
|
XM_017018398.2:c.1738G=
|
XP_016873887.1:p.Ala580=
|
|
|
XM_017018399.1:c.1198G=
|
XP_016873888.1:p.Ala400=
|
|
|
NM_031471.6:c.1738G=
MANE Select
|
NP_113659.3:p.Ala580=
|
|
|
NM_001382361.1:c.1738G=
|
NP_001369290.1:p.Ala580=
|
|
|
NM_001382362.1:c.1750G=
|
NP_001369291.1:p.Ala584=
|
|
|
NM_001382363.1:c.1198G=
|
NP_001369292.1:p.Ala400=
|
|
|
NM_001382364.1:c.1210G=
|
NP_001369293.1:p.Ala404=
|
|
|
NM_001382448.1:c.1738G=
|
NP_001369377.1:p.Ala580=
|
|
|
NM_178443.3:c.1750G=
|
NP_848537.1:p.Ala584=
|
|
