ENST00000342245.9:c.*271G>T
MANE Select
|
ENSP00000340409.4:n.*271G>T
|
|
ENST00000342245.8:c.*271G>T
|
ENSP00000340409.4:n.*271G>T
|
|
ENST00000526280.1:c.1224G>T
|
|
|
ENST00000533123.5:c.*894G>T
|
ENSP00000435950.1:n.*894G>T
|
|
ENST00000534405.5:c.*998G>T
|
ENSP00000434353.1:n.*998G>T
|
|
NM_000543.4:c.*271G>T
|
NP_000534.3:n.*271G>T
|
|
NM_001007593.2:c.*271G>T
|
NP_001007594.2:n.*271G>T
|
|
XM_011520303.1:c.*271G>T
|
XP_011518605.1:n.*271G>T
|
|
NM_001318087.1:c.*660G>T
|
NP_001305016.1:n.*660G>T
|
|
NM_001318088.1:c.*271G>T
|
NP_001305017.1:n.*271G>T
|
|
NM_001365135.1:c.*271G>T
|
NP_001352064.1:n.*271G>T
|
|
NR_027400.2:n.2180G>T
|
|
|
NR_134502.1:n.1719G>T
|
|
|
XR_001747940.2:n.2352G>T
|
|
|
XR_002957158.1:n.2534G>T
|
|
|
NM_000543.5:c.*271G>T
MANE Select
|
NP_000534.3:n.*271G>T
|
|
NM_001007593.3:c.*271G>T
|
NP_001007594.2:n.*271G>T
|
|
NM_001318087.2:c.*660G>T
|
NP_001305016.1:n.*660G>T
|
|
NM_001318088.2:c.*271G>T
|
NP_001305017.1:n.*271G>T
|
|
NM_001365135.2:c.*271G>T
|
NP_001352064.1:n.*271G>T
|
|
NR_027400.3:n.2120G>T
|
|
|
NR_134502.2:n.1659G>T
|
|
|