ENST00000328300.11:c.2756C>A
MANE Select
|
ENSP00000331902.7:p.Pro919His
|
|
ENST00000361603.7:c.2756C>A
|
ENSP00000354505.2:p.Pro919His
|
|
ENST00000328300.10:c.2756C>A
|
ENSP00000331902.6:p.Pro919His
|
|
ENST00000361603.6:c.2756C>A
|
ENSP00000354505.2:p.Pro919His
|
|
ENST00000483338.1:n.2212C>A
|
|
|
NM_000495.4:c.2756C>A
|
NP_000486.1:p.Pro919His
|
|
NM_033380.2:c.2756C>A
|
NP_203699.1:p.Pro919His
|
|
XM_005262070.2:c.2756C>A
|
XP_005262127.1:p.Pro919His
|
|
XM_005262072.3:c.2756C>A
|
XP_005262129.1:p.Pro919His
|
|
XM_006724616.2:c.2756C>A
|
XP_006724679.1:p.Pro919His
|
|
XM_011530849.1:c.2432C>A
|
XP_011529151.1:p.Pro811His
|
|
XM_011530850.1:c.2756C>A
|
XP_011529152.1:p.Pro919His
|
|
XM_011530851.1:c.329C>A
|
XP_011529153.1:p.Pro110His
|
|
XM_011530849.2:c.2771C>A
|
XP_011529151.2:p.Pro924His
|
|
XM_017029259.2:c.2771C>A
|
XP_016884748.1:p.Pro924His
|
|
XM_017029260.1:c.2771C>A
|
XP_016884749.1:p.Pro924His
|
|
XM_017029261.1:c.2771C>A
|
XP_016884750.1:p.Pro924His
|
|
XM_017029262.2:c.2771C>A
|
XP_016884751.1:p.Pro924His
|
|
XM_017029263.2:c.1091C>A
|
XP_016884752.1:p.Pro364His
|
|
NM_000495.5:c.2756C>A
|
NP_000486.1:p.Pro919His
|
|
NM_033380.3:c.2756C>A
MANE Select
|
NP_203699.1:p.Pro919His
|
|