ENST00000355112.8:c.3926G>T
MANE Select
|
ENSP00000347232.3:p.Arg1309Ile
|
|
ENST00000560559.2:n.2499G>T
|
|
|
ENST00000648453.1:c.3926G>T
|
ENSP00000497646.1:p.Arg1309Ile
|
|
ENST00000680772.1:c.3926G>T
|
ENSP00000506117.1:p.Arg1309Ile
|
|
ENST00000681142.1:c.3926G>T
|
ENSP00000506682.1:p.Arg1309Ile
|
|
ENST00000355112.7:c.3926G>T
|
ENSP00000347232.3:p.Arg1309Ile
|
|
ENST00000558825.5:n.1273G>T
|
|
|
ENST00000559724.5:c.*2850G>T
|
ENSP00000453359.1:n.*2850G>T
|
|
ENST00000560136.5:n.1952G>T
|
|
|
ENST00000560509.5:c.3533G>T
|
ENSP00000454158.1:p.Arg1178Ile
|
|
ENST00000560821.1:n.346G>T
|
|
|
NM_000057.3:c.3926G>T
|
NP_000048.1:p.Arg1309Ile
|
|
NM_001287246.1:c.3926G>T
|
NP_001274175.1:p.Arg1309Ile
|
|
NM_001287247.1:c.3533G>T
|
NP_001274176.1:p.Arg1178Ile
|
|
NM_001287248.1:c.2801G>T
|
NP_001274177.1:p.Arg934Ile
|
|
XM_006720632.2:c.1964G>T
|
XP_006720695.1:p.Arg655Ile
|
|
XM_011521881.1:c.2612G>T
|
XP_011520183.1:p.Arg871Ile
|
|
XM_011521881.2:c.2612G>T
|
XP_011520183.1:p.Arg871Ile
|
|
NM_000057.4:c.3926G>T
MANE Select
|
NP_000048.1:p.Arg1309Ile
|
|
NM_001287246.2:c.3926G>T
|
NP_001274175.1:p.Arg1309Ile
|
|
NM_001287247.2:c.3533G>T
|
NP_001274176.1:p.Arg1178Ile
|
|
NM_001287248.2:c.2801G>T
|
NP_001274177.1:p.Arg934Ile
|
|