ENST00000496887.7:c.1104G>C
(KCNQ1)
|
ENSP00000434560.2:p.Glu368Asp
|
|
ENST00000646564.2:c.921G>C
(KCNQ1)
|
ENSP00000495806.2:p.Glu307Asp
|
|
ENST00000155840.12:c.1461G>C
(KCNQ1)
MANE Select
|
ENSP00000155840.2:p.Glu487Asp
|
|
ENST00000335475.6:c.1080G>C
(KCNQ1)
|
ENSP00000334497.5:p.Glu360Asp
|
|
ENST00000646564.1:c.567G>C
(KCNQ1)
|
ENSP00000495806.1:p.Glu189Asp
|
|
ENST00000155840.9:c.1461G>C
(KCNQ1)
|
ENSP00000155840.2:p.Glu487Asp
|
|
ENST00000335475.5:c.1080G>C
(KCNQ1)
|
ENSP00000334497.5:p.Glu360Asp
|
|
NM_000218.2:c.1461G>C , LRG_287t1:c.1461G>C
(KCNQ1)
|
NP_000209.2:p.Glu487Asp
|
|
NM_181798.1:c.1080G>C , LRG_287t2:c.1080G>C
(KCNQ1)
|
NP_861463.1:p.Glu360Asp
|
|
NR_002728.3:n.37971C>G
(KCNQ1OT1)
|
|
|
NM_000218.3:c.1461G>C
(KCNQ1)
MANE Select
|
NP_000209.2:p.Glu487Asp
|
|