ENST00000299506.3:c.165G>A
MANE Select
|
ENSP00000299506.3:p.Arg55=
|
|
ENST00000299506.2:c.165G>A
|
ENSP00000299506.2:p.Arg55=
|
|
ENST00000305253.8:c.330G>A
|
ENSP00000305426.4:p.Arg110=
|
|
ENST00000534099.5:c.183G>A
|
ENSP00000434400.1:p.Arg61=
|
|
NM_003320.4:c.330G>A
|
NP_003311.2:p.Arg110=
|
|
NM_177972.2:c.165G>A
|
NP_813977.1:p.Arg55=
|
|
XM_005253109.2:c.291G>A
|
XP_005253166.1:p.Arg97=
|
|
XM_011520344.1:c.201G>A
|
XP_011518646.1:p.Arg67=
|
|
XM_005253109.3:c.291G>A
|
XP_005253166.1:p.Arg97=
|
|
XM_011520344.2:c.201G>A
|
XP_011518646.1:p.Arg67=
|
|
NM_177972.3:c.165G>A
MANE Select
|
NP_813977.1:p.Arg55=
|
|
NM_003320.5:c.330G>A
|
NP_003311.2:p.Arg110=
|
|