ENST00000496887.7:c.1588G>T
(KCNQ1)
|
ENSP00000434560.2:p.Asp530Tyr
|
|
ENST00000155840.12:c.1945G>T
(KCNQ1)
MANE Select
|
ENSP00000155840.2:p.Asp649Tyr
|
|
ENST00000335475.6:c.1564G>T
(KCNQ1)
|
ENSP00000334497.5:p.Asp522Tyr
|
|
ENST00000526095.2:c.349G>T
(KCNQ1)
|
ENSP00000494939.1:p.Asp117Tyr
|
|
ENST00000155840.9:c.1945G>T
(KCNQ1)
|
ENSP00000155840.2:p.Asp649Tyr
|
|
ENST00000335475.5:c.1564G>T
(KCNQ1)
|
ENSP00000334497.5:p.Asp522Tyr
|
|
ENST00000526095.1:n.452G>T
(KCNQ1)
|
|
|
NM_000218.2:c.1945G>T , LRG_287t1:c.1945G>T
(KCNQ1)
|
NP_000209.2:p.Asp649Tyr
|
|
NM_181798.1:c.1564G>T , LRG_287t2:c.1564G>T
(KCNQ1)
|
NP_861463.1:p.Asp522Tyr
|
|
NR_130721.1:n.778-7475C>A
(KCNQ1-AS1)
|
|
|
NM_000218.3:c.1945G>T
(KCNQ1)
MANE Select
|
NP_000209.2:p.Asp649Tyr
|
|