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ENST00000279227.10:c.1345A=
|
ENSP00000279227.5:p.Met449=
|
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ENST00000540554.2:n.2511A=
|
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|
|
ENST00000541252.2:c.793A=
|
ENSP00000438885.2:p.Met265=
|
|
|
ENST00000541326.6:n.754A=
|
|
|
|
ENST00000544997.6:c.1333A=
|
ENSP00000445778.2:p.Met445=
|
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|
ENST00000545896.2:c.22A=
|
ENSP00000440209.2:p.Met8=
|
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|
ENST00000546255.2:n.1637A=
|
|
|
|
ENST00000698845.1:c.*528A=
|
ENSP00000513981.1:n.*528A=
|
|
|
ENST00000698846.1:n.1579A=
|
|
|
|
ENST00000698847.1:c.*738A=
|
ENSP00000513982.1:n.*738A=
|
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ENST00000698848.1:n.631A=
|
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ENST00000698849.1:n.453A=
|
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ENST00000698850.1:n.1101A=
|
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|
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ENST00000698852.1:c.1333A=
|
ENSP00000513984.1:p.Met445=
|
|
|
ENST00000698853.1:c.*562A=
|
ENSP00000513985.1:n.*562A=
|
|
|
ENST00000698854.1:c.*663A=
|
ENSP00000513986.1:n.*663A=
|
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ENST00000698855.1:n.2985A=
|
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ENST00000698856.1:n.2679A=
|
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ENST00000698859.1:n.1497A=
|
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|
|
ENST00000698860.1:c.1345A=
|
ENSP00000513988.1:p.Met449=
|
|
|
ENST00000698861.1:c.1333A=
|
ENSP00000513989.1:p.Met445=
|
|
|
ENST00000698862.1:c.*629A=
|
ENSP00000513990.1:n.*629A=
|
|
|
ENST00000698863.1:c.1333A=
|
ENSP00000513991.1:p.Met445=
|
|
|
ENST00000698864.1:n.1548A=
|
|
|
|
ENST00000698865.1:c.1354A=
|
ENSP00000513992.1:p.Met452=
|
|
|
ENST00000698866.1:c.*847A=
|
ENSP00000513993.1:n.*847A=
|
|
|
ENST00000698867.1:n.5308A=
|
|
|
|
ENST00000698868.1:c.1198A=
|
ENSP00000513994.1:p.Met400=
|
|
|
ENST00000698869.1:c.1311+131A=
|
ENSP00000513995.1:n.1311+131A=
|
|
|
ENST00000698870.1:c.1333A=
|
ENSP00000513996.1:p.Met445=
|
|
|
ENST00000698871.1:n.1856A=
|
|
|
|
ENST00000698872.1:c.*122A=
|
ENSP00000513997.1:n.*122A=
|
|
|
ENST00000698873.1:c.*528A=
|
ENSP00000513998.1:n.*528A=
|
|
|
ENST00000698874.1:c.793A=
|
ENSP00000513999.1:p.Met265=
|
|
|
ENST00000698875.1:n.1193A=
|
|
|
|
ENST00000698876.1:n.1381A=
|
|
|
|
ENST00000698877.1:n.901A=
|
|
|
|
ENST00000698878.1:c.1327A=
|
ENSP00000514000.1:p.Met443=
|
|
|
ENST00000698880.1:c.1201A=
|
|
|
|
ENST00000345728.10:c.1333A=
MANE Select
|
ENSP00000339950.5:p.Met445=
|
|
|
ENST00000279227.9:c.1345A=
|
ENSP00000279227.5:p.Met449=
|
|
|
ENST00000345728.9:c.1333A=
|
ENSP00000339950.5:p.Met445=
|
|
|
ENST00000541326.5:n.749A=
|
|
|
|
ENST00000545896.1:c.21A=
|
ENSP00000440209.1:p.Gly7=
|
|
|
NM_031471.5:c.1333A=
|
NP_113659.3:p.Met445=
|
|
|
NM_178443.2:c.1345A= , LRG_180t1:c.1345A=
|
NP_848537.1:p.Met449=
|
|
|
XM_011545294.1:c.1345A=
|
XP_011543596.1:p.Met449=
|
|
|
XM_011545295.1:c.805A=
|
XP_011543597.1:p.Met269=
|
|
|
XM_011545296.1:c.805A=
|
XP_011543598.1:p.Met269=
|
|
|
XM_011545294.3:c.1345A=
|
XP_011543596.1:p.Met449=
|
|
|
XM_011545295.2:c.805A=
|
XP_011543597.1:p.Met269=
|
|
|
XM_017018398.2:c.1333A=
|
XP_016873887.1:p.Met445=
|
|
|
XM_017018399.1:c.793A=
|
XP_016873888.1:p.Met265=
|
|
|
NM_031471.6:c.1333A=
MANE Select
|
NP_113659.3:p.Met445=
|
|
|
NM_001382361.1:c.1333A=
|
NP_001369290.1:p.Met445=
|
|
|
NM_001382362.1:c.1345A=
|
NP_001369291.1:p.Met449=
|
|
|
NM_001382363.1:c.793A=
|
NP_001369292.1:p.Met265=
|
|
|
NM_001382364.1:c.805A=
|
NP_001369293.1:p.Met269=
|
|
|
NM_001382448.1:c.1333A=
|
NP_001369377.1:p.Met445=
|
|
|
NM_178443.3:c.1345A=
|
NP_848537.1:p.Met449=
|
|
