ENST00000260947.9:c.*263G>C
MANE Select
|
ENSP00000260947.4:n.*263G>C
|
|
ENST00000260947.8:c.*263G>C
|
ENSP00000260947.4:n.*263G>C
|
|
ENST00000613374.4:c.*263G>C
|
ENSP00000484464.1:n.*263G>C
|
|
ENST00000613706.4:c.*263G>C
|
ENSP00000484976.1:n.*263G>C
|
|
ENST00000617164.4:c.*263G>C
|
ENSP00000480470.1:n.*263G>C
|
|
ENST00000619009.4:c.*263G>C
|
ENSP00000482293.1:n.*263G>C
|
|
NM_000465.3:c.*263G>C
|
NP_000456.2:n.*263G>C
|
|
NM_001282543.1:c.*263G>C
|
NP_001269472.1:n.*263G>C
|
|
NM_001282545.1:c.*263G>C
|
NP_001269474.1:n.*263G>C
|
|
NM_001282548.1:c.*263G>C
|
NP_001269477.1:n.*263G>C
|
|
NM_001282549.1:c.*263G>C
|
NP_001269478.1:n.*263G>C
|
|
NR_104212.1:n.2590G>C
|
|
|
NR_104215.1:n.2533G>C
|
|
|
NR_104216.1:n.1789G>C
|
|
|
XM_011511567.1:c.*263G>C
|
XP_011509869.1:n.*263G>C
|
|
XM_017004613.1:c.*263G>C
|
XP_016860102.1:n.*263G>C
|
|
NM_000465.4:c.*263G>C
MANE Select
|
NP_000456.2:n.*263G>C
|
|
NM_001282543.2:c.*263G>C
|
NP_001269472.1:n.*263G>C
|
|
NM_001282545.2:c.*263G>C
|
NP_001269474.1:n.*263G>C
|
|
NM_001282548.2:c.*263G>C
|
NP_001269477.1:n.*263G>C
|
|
NM_001282549.2:c.*263G>C
|
NP_001269478.1:n.*263G>C
|
|
NR_104212.2:n.2562G>C
|
|
|
NR_104215.2:n.2505G>C
|
|
|
NR_104216.2:n.1761G>C
|
|
|