|
NM_032608.7:c.5207G>A
MANE Select
|
NP_115997.5:p.Arg1736His
|
|
ENST00000335473.12:c.5207G>A
MANE Select
|
ENSP00000334563.8:p.Arg1736His
|
|
NM_001318245.1:c.5210G>A
|
NP_001305174.1:p.Arg1737His
|
|
NM_001318245.2:c.5210G>A
|
NP_001305174.1:p.Arg1737His
|
|
NM_032608.5:c.5207G>A
|
NP_115997.5:p.Arg1736His
|
|
NM_032608.6:c.5207G>A
|
NP_115997.5:p.Arg1736His
|
|
ENST00000335473.11:c.5207G>A
|
ENSP00000334563.7:p.Arg1736His
|
|
ENST00000407587.6:c.5210G>A
|
ENSP00000386096.2:p.Arg1737His
|
|
ENST00000418374.6:n.3778G>A
|
|
|
ENST00000536101.5:c.5207G>A
|
ENSP00000441229.1:p.Arg1736His
|
|
ENST00000539302.5:c.*2665G>A
|
ENSP00000437587.1:n.*2665G>A
|
|
XM_005261786.3:c.5210G>A
|
XP_005261843.1:p.Arg1737His
|
|
XM_011530458.1:c.5336G>A
|
XP_011528760.1:p.Arg1779His
|
|
XM_011530458.2:c.5336G>A
|
XP_011528760.1:p.Arg1779His
|
|
XM_011530459.1:c.5336G>A
|
XP_011528761.1:p.Arg1779His
|
|
XM_011530459.2:c.5336G>A
|
XP_011528761.1:p.Arg1779His
|
|
XM_011530460.1:c.5336G>A
|
XP_011528762.1:p.Arg1779His
|
|
XM_011530460.2:c.5336G>A
|
XP_011528762.1:p.Arg1779His
|
|
XM_011530461.1:c.5336G>A
|
XP_011528763.1:p.Arg1779His
|
|
XM_011530461.2:c.5336G>A
|
XP_011528763.1:p.Arg1779His
|
|
XM_011530462.1:c.5336G>A
|
XP_011528764.1:p.Arg1779His
|
|
XM_011530463.1:c.5336G>A
|
XP_011528765.1:p.Arg1779His
|
|
XM_011530464.1:c.5333G>A
|
XP_011528766.1:p.Arg1778His
|
|
XM_011530464.2:c.5333G>A
|
XP_011528766.1:p.Arg1778His
|
|
XM_011530465.1:c.4853G>A
|
XP_011528767.1:p.Arg1618His
|
|
XM_011530465.2:c.4853G>A
|
XP_011528767.1:p.Arg1618His
|
|
XM_011530466.1:c.5336G>A
|
XP_011528768.1:p.Arg1779His
|
|
XM_011530466.2:c.5336G>A
|
XP_011528768.1:p.Arg1779His
|
|
XM_017029012.1:c.5336G>A
|
XP_016884501.1:p.Arg1779His
|
|
XM_017029013.1:c.5336G>A
|
XP_016884502.1:p.Arg1779His
|
|
XM_017029014.1:c.5333G>A
|
XP_016884503.1:p.Arg1778His
|
|
XM_017029015.1:c.5204G>A
|
XP_016884504.1:p.Arg1735His
|
|
XM_017029016.1:c.2672G>A
|
XP_016884505.1:p.Arg891His
|
|
XM_017029017.1:c.2669G>A
|
XP_016884506.1:p.Arg890His
|
