ENST00000303415.7:c.*2+211A>G
MANE Select
|
ENSP00000305529.3:n.*2+211A>G
|
|
ENST00000344103.8:c.*2+211A>G
|
ENSP00000342759.4:n.*2+211A>G
|
|
ENST00000381580.5:c.*2+211A>G
|
ENSP00000370992.1:n.*2+211A>G
|
|
ENST00000381583.6:c.*2+211A>G
|
ENSP00000370995.2:n.*2+211A>G
|
|
ENST00000478145.6:n.227+211A>G
|
|
|
ENST00000497407.2:n.315+211A>G
|
|
|
NM_001039508.1:c.*2+211A>G
|
NP_001034597.1:n.*2+211A>G
|
|
NM_018556.3:c.*2+211A>G
|
NP_061026.2:n.*2+211A>G
|
|
NM_080816.2:c.*2+211A>G
|
NP_543006.2:n.*2+211A>G
|
|
XM_005260749.2:c.*2+211A>G
|
XP_005260806.1:n.*2+211A>G
|
|
XM_011529286.1:c.*2+211A>G
|
XP_011527588.1:n.*2+211A>G
|
|
XM_005260749.4:c.*2+211A>G
|
XP_005260806.1:n.*2+211A>G
|
|
XM_011529286.2:c.*2+211A>G
|
XP_011527588.1:n.*2+211A>G
|
|
NM_018556.4:c.*2+211A>G
MANE Select
|
NP_061026.2:n.*2+211A>G
|
|
NM_080816.3:c.*2+211A>G
|
NP_543006.2:n.*2+211A>G
|
|
NM_001039508.2:c.*2+211A>G
|
NP_001034597.1:n.*2+211A>G
|
|