|
NM_000218.3:c.1863T>A
(KCNQ1)
MANE Select
|
NP_000209.2:p.Gly621=
|
|
ENST00000155840.12:c.1863T>A
(KCNQ1)
MANE Select
|
ENSP00000155840.2:p.Gly621=
|
|
NM_000218.2:c.1863T>A , LRG_287t1:c.1863T>A
(KCNQ1)
|
NP_000209.2:p.Gly621=
|
|
NM_181798.1:c.1482T>A , LRG_287t2:c.1482T>A
(KCNQ1)
|
NP_861463.1:p.Gly494=
|
|
NR_130721.1:n.778-7393A>T
(KCNQ1-AS1)
|
|
|
ENST00000155840.9:c.1863T>A
(KCNQ1)
|
ENSP00000155840.2:p.Gly621=
|
|
ENST00000335475.5:c.1482T>A
(KCNQ1)
|
ENSP00000334497.5:p.Gly494=
|
|
ENST00000335475.6:c.1482T>A
(KCNQ1)
|
ENSP00000334497.5:p.Gly494=
|
|
ENST00000496887.7:c.1506T>A
(KCNQ1)
|
ENSP00000434560.2:p.Gly502=
|
|
ENST00000526095.1:n.370T>A
(KCNQ1)
|
|
|
ENST00000526095.2:c.267T>A
(KCNQ1)
|
ENSP00000494939.1:p.Gly89=
|
