NM_002062.5:c.502G=
MANE Select
|
NP_002053.3:p.Gly168=
|
ENST00000373256.5:c.502G=
MANE Select
|
ENSP00000362353.4:p.Gly168=
|
NM_002062.3:c.502G=
|
NP_002053.3:p.Gly168=
|
NM_002062.4:c.502G=
|
NP_002053.3:p.Gly168=
|
NR_136562.1:n.562G=
|
|
NR_136562.2:n.562G=
|
|
NR_136563.1:n.562G=
|
|
NR_136563.2:n.562G=
|
|
ENST00000373256.4:c.502G=
|
ENSP00000362353.4:p.Gly168=
|
XM_017010750.1:c.517G=
|
XP_016866239.1:p.Gly173=
|
XM_017010751.1:c.517G=
|
XP_016866240.1:p.Gly173=
|
XR_001743346.1:n.1097G=
|
|
XR_001743347.1:n.1097G=
|
|
XR_001743348.1:n.1097G=
|
|
XR_926153.1:n.562G=
|
|
XR_926154.1:n.562G=
|
|
XR_926155.1:n.562G=
|
|