ENST00000642496.1:c.4000A>G
|
|
|
ENST00000644397.2:c.5141A>G
MANE Select
|
ENSP00000495195.1:p.His1714Arg
|
|
ENST00000373965.6:c.4952A>G
|
ENSP00000363076.3:p.His1651Arg
|
|
ENST00000414778.5:c.4949A>G
|
ENSP00000410304.2:p.His1650Arg
|
|
ENST00000495484.5:c.1169A>G
|
ENSP00000480780.1:p.His390Arg
|
|
ENST00000614895.4:c.4964A>G
|
ENSP00000478512.1:p.His1655Arg
|
|
ENST00000616114.4:c.4946A>G
|
ENSP00000483745.1:p.His1649Arg
|
|
ENST00000618301.4:c.1301A>G
|
ENSP00000482780.1:p.His434Arg
|
|
ENST00000621708.4:c.4967A>G
|
ENSP00000484454.1:p.His1656Arg
|
|
NM_001142771.1:c.4967A>G
|
NP_001136243.1:p.His1656Arg
|
|
NM_001142772.1:c.4952A>G
|
NP_001136244.1:p.His1651Arg
|
|
NM_001354420.1:c.4946A>G
|
NP_001341349.1:p.His1649Arg
|
|
NM_001354429.1:c.5075A>G
|
NP_001341358.1:p.His1692Arg
|
|
XR_001747192.2:n.11433A>G
|
|
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XR_001747193.2:n.11424A>G
|
|
|
NM_001142771.2:c.4967A>G
|
NP_001136243.1:p.His1656Arg
|
|
NM_001142772.2:c.4952A>G
|
NP_001136244.1:p.His1651Arg
|
|
NM_001354420.2:c.4946A>G
|
NP_001341349.1:p.His1649Arg
|
|
NM_001354429.2:c.5075A>G
|
NP_001341358.1:p.His1692Arg
|
|
NM_001384140.1:c.5141A>G
MANE Select
|
NP_001371069.1:p.His1714Arg
|
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