ENST00000342245.9:c.*266G>T
MANE Select
|
ENSP00000340409.4:n.*266G>T
|
|
ENST00000342245.8:c.*266G>T
|
ENSP00000340409.4:n.*266G>T
|
|
ENST00000526280.1:c.1219G>T
|
|
|
ENST00000533123.5:c.*889G>T
|
ENSP00000435950.1:n.*889G>T
|
|
ENST00000534405.5:c.*993G>T
|
ENSP00000434353.1:n.*993G>T
|
|
NM_000543.4:c.*266G>T
|
NP_000534.3:n.*266G>T
|
|
NM_001007593.2:c.*266G>T
|
NP_001007594.2:n.*266G>T
|
|
XM_011520303.1:c.*266G>T
|
XP_011518605.1:n.*266G>T
|
|
NM_001318087.1:c.*655G>T
|
NP_001305016.1:n.*655G>T
|
|
NM_001318088.1:c.*266G>T
|
NP_001305017.1:n.*266G>T
|
|
NM_001365135.1:c.*266G>T
|
NP_001352064.1:n.*266G>T
|
|
NR_027400.2:n.2175G>T
|
|
|
NR_134502.1:n.1714G>T
|
|
|
XR_001747940.2:n.2347G>T
|
|
|
XR_002957158.1:n.2529G>T
|
|
|
NM_000543.5:c.*266G>T
MANE Select
|
NP_000534.3:n.*266G>T
|
|
NM_001007593.3:c.*266G>T
|
NP_001007594.2:n.*266G>T
|
|
NM_001318087.2:c.*655G>T
|
NP_001305016.1:n.*655G>T
|
|
NM_001318088.2:c.*266G>T
|
NP_001305017.1:n.*266G>T
|
|
NM_001365135.2:c.*266G>T
|
NP_001352064.1:n.*266G>T
|
|
NR_027400.3:n.2115G>T
|
|
|
NR_134502.2:n.1654G>T
|
|
|