ENST00000496887.7:c.1116G>T
(KCNQ1)
|
ENSP00000434560.2:p.Leu372=
|
|
ENST00000646564.2:c.933G>T
(KCNQ1)
|
ENSP00000495806.2:p.Leu311=
|
|
ENST00000155840.12:c.1473G>T
(KCNQ1)
MANE Select
|
ENSP00000155840.2:p.Leu491=
|
|
ENST00000335475.6:c.1092G>T
(KCNQ1)
|
ENSP00000334497.5:p.Leu364=
|
|
ENST00000646564.1:c.579G>T
(KCNQ1)
|
ENSP00000495806.1:p.Leu193=
|
|
ENST00000155840.9:c.1473G>T
(KCNQ1)
|
ENSP00000155840.2:p.Leu491=
|
|
ENST00000335475.5:c.1092G>T
(KCNQ1)
|
ENSP00000334497.5:p.Leu364=
|
|
NM_000218.2:c.1473G>T , LRG_287t1:c.1473G>T
(KCNQ1)
|
NP_000209.2:p.Leu491=
|
|
NM_181798.1:c.1092G>T , LRG_287t2:c.1092G>T
(KCNQ1)
|
NP_861463.1:p.Leu364=
|
|
NR_002728.3:n.37959C>A
(KCNQ1OT1)
|
|
|
NM_000218.3:c.1473G>T
(KCNQ1)
MANE Select
|
NP_000209.2:p.Leu491=
|
|