ENST00000372748.8:c.1045G>C
MANE Select
|
ENSP00000361834.3:p.Gly349Arg
|
|
ENST00000372748.7:c.1045G>C
|
ENSP00000361834.3:p.Gly349Arg
|
|
ENST00000482722.5:n.1348G>C
|
|
|
NM_001852.3:c.1045G>C
|
NP_001843.1:p.Gly349Arg
|
|
XM_006710365.2:c.1045G>C
|
XP_006710428.1:p.Gly349Arg
|
|
XM_011540714.1:c.1057G>C
|
XP_011539016.1:p.Gly353Arg
|
|
XM_011540715.1:c.775G>C
|
XP_011539017.1:p.Gly259Arg
|
|
XM_011540716.1:c.775G>C
|
XP_011539018.1:p.Gly259Arg
|
|
XM_011540717.1:c.502G>C
|
XP_011539019.1:p.Gly168Arg
|
|
XM_006710365.3:c.1045G>C
|
XP_006710428.1:p.Gly349Arg
|
|
XM_011540715.2:c.775G>C
|
XP_011539017.1:p.Gly259Arg
|
|
XM_011540716.2:c.775G>C
|
XP_011539018.1:p.Gly259Arg
|
|
XM_011540717.2:c.502G>C
|
XP_011539019.1:p.Gly168Arg
|
|
XM_017000332.1:c.1057G>C
|
XP_016855821.1:p.Gly353Arg
|
|
XM_017000333.1:c.763G>C
|
XP_016855822.1:p.Gly255Arg
|
|
NM_001852.4:c.1045G>C
MANE Select
|
NP_001843.1:p.Gly349Arg
|
|