ENST00000356231.4:c.2645+46T>A
MANE Select
|
ENSP00000348564.3:n.2645+46T>A
|
|
ENST00000643434.1:c.*1823+46T>A
|
ENSP00000494699.1:n.*1823+46T>A
|
|
ENST00000356231.3:c.2645+46T>A
|
ENSP00000348564.3:n.2645+46T>A
|
|
ENST00000562465.5:c.638+46T>A
|
ENSP00000454246.1:n.638+46T>A
|
|
NM_138477.2:c.2645+46T>A
|
NP_612486.2:n.2645+46T>A
|
|
XM_005254176.3:c.2648+46T>A
|
XP_005254233.1:n.2648+46T>A
|
|
XM_011521270.1:c.2672+46T>A
|
XP_011519572.1:n.2672+46T>A
|
|
XM_011521271.1:c.2669+46T>A
|
XP_011519573.1:n.2669+46T>A
|
|
XM_011521272.1:c.2672+46T>A
|
XP_011519574.1:n.2672+46T>A
|
|
XM_011521273.1:c.2672+46T>A
|
XP_011519575.1:n.2672+46T>A
|
|
XM_011521274.1:c.1637+46T>A
|
XP_011519576.1:n.1637+46T>A
|
|
XM_011521275.1:c.1889+46T>A
|
XP_011519577.1:n.1889+46T>A
|
|
NM_138477.4:c.2645+46T>A
MANE Select
|
NP_612486.2:n.2645+46T>A
|
|
XM_005254176.5:c.2648+46T>A
|
XP_005254233.1:n.2648+46T>A
|
|
XM_011521270.2:c.2672+46T>A
|
XP_011519572.1:n.2672+46T>A
|
|
XM_011521271.2:c.2669+46T>A
|
XP_011519573.1:n.2669+46T>A
|
|
XM_011521274.2:c.1637+46T>A
|
XP_011519576.1:n.1637+46T>A
|
|
XR_001751104.1:n.2702+46T>A
|
|
|
XR_001751105.1:n.2702+46T>A
|
|
|