ENST00000299506.3:c.177G>T
MANE Select
|
ENSP00000299506.3:p.Arg59=
|
|
ENST00000299506.2:c.177G>T
|
ENSP00000299506.2:p.Arg59=
|
|
ENST00000305253.8:c.342G>T
|
ENSP00000305426.4:p.Arg114=
|
|
ENST00000534099.5:c.195G>T
|
ENSP00000434400.1:p.Arg65=
|
|
NM_003320.4:c.342G>T
|
NP_003311.2:p.Arg114=
|
|
NM_177972.2:c.177G>T
|
NP_813977.1:p.Arg59=
|
|
XM_005253109.2:c.303G>T
|
XP_005253166.1:p.Arg101=
|
|
XM_011520344.1:c.213G>T
|
XP_011518646.1:p.Arg71=
|
|
XM_005253109.3:c.303G>T
|
XP_005253166.1:p.Arg101=
|
|
XM_011520344.2:c.213G>T
|
XP_011518646.1:p.Arg71=
|
|
NM_177972.3:c.177G>T
MANE Select
|
NP_813977.1:p.Arg59=
|
|
NM_003320.5:c.342G>T
|
NP_003311.2:p.Arg114=
|
|