|
NM_000458.4:c.1046-9770A=
MANE Select
|
NP_000449.1:n.1046-9770A=
|
|
ENST00000617811.5:c.1046-9770A=
MANE Select
|
ENSP00000480291.1:n.1046-9770A=
|
|
NM_000458.3:c.1046-9770A=
|
NP_000449.1:n.1046-9770A=
|
|
NM_001165923.3:c.968-9770A=
|
NP_001159395.1:n.968-9770A=
|
|
NM_001165923.4:c.968-9770A=
|
NP_001159395.1:n.968-9770A=
|
|
NM_001304286.1:c.968-9770A=
|
NP_001291215.1:n.968-9770A=
|
|
NM_001304286.2:c.968-9770A=
|
NP_001291215.1:n.968-9770A=
|
|
ENST00000613727.4:c.968-9770A=
|
ENSP00000477524.1:n.968-9770A=
|
|
ENST00000614313.4:c.1046-9770A=
|
ENSP00000482529.1:n.1046-9770A=
|
|
ENST00000617272.4:c.1046-9770A=
|
ENSP00000478682.1:n.1046-9770A=
|
|
ENST00000617811.4:c.1046-9770A=
|
ENSP00000480291.1:n.1046-9770A=
|
|
ENST00000621123.4:c.968-9770A=
|
ENSP00000482711.1:n.968-9770A=
|
|
XM_011525160.1:c.1046-9770A=
|
XP_011523462.1:n.1046-9770A=
|
|
XM_011525161.1:c.1046-9770A=
|
XP_011523463.1:n.1046-9770A=
|
|
XM_011525162.2:c.*414A=
|
XP_011523464.1:n.*414A=
|
|
XM_011525164.1:c.968-9770A=
|
XP_011523466.1:n.968-9770A=
|
|
XR_001752875.1:n.574+2947T=
|
|
|
XR_934718.1:n.2236-3432T=
|
|
