ENST00000342245.9:c.1719G>T
MANE Select
|
ENSP00000340409.4:p.Trp573Cys
|
|
ENST00000342245.8:c.1719G>T
|
ENSP00000340409.4:p.Trp573Cys
|
|
ENST00000526280.1:c.776G>T
|
|
|
ENST00000527275.5:c.1716G>T
|
ENSP00000435350.1:p.Trp572Cys
|
|
ENST00000531303.5:c.*570G>T
|
ENSP00000432625.1:n.*570G>T
|
|
ENST00000533123.5:c.*446G>T
|
ENSP00000435950.1:n.*446G>T
|
|
ENST00000534405.5:c.*550G>T
|
ENSP00000434353.1:n.*550G>T
|
|
NM_000543.4:c.1719G>T
|
NP_000534.3:p.Trp573Cys
|
|
NM_001007593.2:c.1716G>T
|
NP_001007594.2:p.Trp572Cys
|
|
XM_005253075.3:c.*212G>T
|
XP_005253132.1:n.*212G>T
|
|
XM_011520303.1:c.1587G>T
|
XP_011518605.1:p.Trp529Cys
|
|
XM_011520304.1:c.*212G>T
|
XP_011518606.1:n.*212G>T
|
|
NM_001318087.1:c.*212G>T
|
NP_001305016.1:n.*212G>T
|
|
NM_001318088.1:c.798G>T
|
NP_001305017.1:p.Trp266Cys
|
|
NM_001365135.1:c.1587G>T
|
NP_001352064.1:p.Trp529Cys
|
|
NR_027400.2:n.1732G>T
|
|
|
NR_134502.1:n.1271G>T
|
|
|
XM_011520304.2:c.*212G>T
|
XP_011518606.1:n.*212G>T
|
|
XR_001747940.2:n.1904G>T
|
|
|
XR_002957158.1:n.2086G>T
|
|
|
NM_000543.5:c.1719G>T
MANE Select
|
NP_000534.3:p.Trp573Cys
|
|
NM_001007593.3:c.1716G>T
|
NP_001007594.2:p.Trp572Cys
|
|
NM_001318087.2:c.*212G>T
|
NP_001305016.1:n.*212G>T
|
|
NM_001318088.2:c.798G>T
|
NP_001305017.1:p.Trp266Cys
|
|
NM_001365135.2:c.1587G>T
|
NP_001352064.1:p.Trp529Cys
|
|
NR_027400.3:n.1672G>T
|
|
|
NR_134502.2:n.1211G>T
|
|
|