ENST00000299084.9:c.1046G>T
MANE Select
|
ENSP00000299084.4:p.Arg349Met
|
|
ENST00000299084.8:c.1046G>T
|
ENSP00000299084.4:p.Arg349Met
|
|
NM_152594.2:c.1046G>T
|
NP_689807.1:p.Arg349Met
|
|
XM_005254202.2:c.1082G>T
|
XP_005254259.1:p.Arg361Met
|
|
XM_005254203.3:c.824G>T
|
XP_005254260.1:p.Arg275Met
|
|
XM_011521288.1:c.983G>T
|
XP_011519590.1:p.Arg328Met
|
|
XM_011521289.1:c.983G>T
|
XP_011519591.1:p.Arg328Met
|
|
XM_011521290.1:c.983G>T
|
XP_011519592.1:p.Arg328Met
|
|
XM_005254202.3:c.1082G>T
|
XP_005254259.1:p.Arg361Met
|
|
XM_011521289.3:c.983G>T
|
XP_011519591.1:p.Arg328Met
|
|
NM_152594.3:c.1046G>T
MANE Select
|
NP_689807.1:p.Arg349Met
|
|