ENST00000328300.11:c.4916A>T
MANE Select
|
ENSP00000331902.7:p.His1639Leu
|
|
ENST00000361603.7:c.4898A>T
|
ENSP00000354505.2:p.His1633Leu
|
|
ENST00000510690.2:n.1410A>T
|
|
|
ENST00000644079.1:n.1747A>T
|
|
|
ENST00000328300.10:c.4916A>T
|
ENSP00000331902.6:p.His1639Leu
|
|
ENST00000361603.6:c.4898A>T
|
ENSP00000354505.2:p.His1633Leu
|
|
ENST00000504541.1:c.219+440A>T
|
ENSP00000424845.1:n.219+440A>T
|
|
ENST00000515658.1:c.325-936A>T
|
|
|
NM_000495.4:c.4898A>T
|
NP_000486.1:p.His1633Leu
|
|
NM_033380.2:c.4916A>T
|
NP_203699.1:p.His1639Leu
|
|
XM_005262070.2:c.4907A>T
|
XP_005262127.1:p.His1636Leu
|
|
XM_006724616.2:c.4916A>T
|
XP_006724679.1:p.His1639Leu
|
|
XM_011530849.1:c.4592A>T
|
XP_011529151.1:p.His1531Leu
|
|
XM_011530851.1:c.2489A>T
|
XP_011529153.1:p.His830Leu
|
|
XM_011530849.2:c.4931A>T
|
XP_011529151.2:p.His1644Leu
|
|
XM_017029259.2:c.4922A>T
|
XP_016884748.1:p.His1641Leu
|
|
XM_017029260.1:c.4913A>T
|
XP_016884749.1:p.His1638Leu
|
|
XM_017029263.2:c.3251A>T
|
XP_016884752.1:p.His1084Leu
|
|
NM_000495.5:c.4898A>T
|
NP_000486.1:p.His1633Leu
|
|
NM_033380.3:c.4916A>T
MANE Select
|
NP_203699.1:p.His1639Leu
|
|