ENST00000331222.6:c.*116G>T
MANE Select
|
ENSP00000328182.4:n.*116G>T
|
|
ENST00000519254.2:c.*116G>T
|
ENSP00000490016.1:n.*116G>T
|
|
ENST00000520991.3:c.*388G>T
|
ENSP00000487905.2:n.*388G>T
|
|
ENST00000635751.1:c.*116G>T
|
ENSP00000489694.1:n.*116G>T
|
|
ENST00000635773.1:c.496+9086G>T
|
|
|
ENST00000635855.1:c.543+9086G>T
|
ENSP00000489726.1:n.543+9086G>T
|
|
ENST00000635970.1:c.*116G>T
|
ENSP00000490439.1:n.*116G>T
|
|
ENST00000636175.1:c.343+9086G>T
|
|
|
ENST00000636934.1:c.543+9086G>T
|
ENSP00000490218.1:n.543+9086G>T
|
|
ENST00000637083.1:c.*116G>T
|
ENSP00000490235.1:n.*116G>T
|
|
ENST00000637156.1:c.*116G>T
|
ENSP00000490458.1:n.*116G>T
|
|
ENST00000331222.4:c.*116G>T
|
ENSP00000328182.4:n.*116G>T
|
|
ENST00000519254.1:n.496G>T
|
|
|
ENST00000523237.1:n.752G>T
|
|
|
NM_018941.3:c.*116G>T , LRG_691t1:c.*116G>T
|
NP_061764.2:n.*116G>T
|
|
XM_005266021.3:c.*116G>T
|
XP_005266078.1:n.*116G>T
|
|
XM_005266022.1:c.*116G>T
|
XP_005266079.1:n.*116G>T
|
|
XM_005266023.1:c.*116G>T
|
XP_005266080.1:n.*116G>T
|
|
XM_011534745.1:c.*116G>T
|
XP_011533047.1:n.*116G>T
|
|
XM_011534746.1:c.*116G>T
|
XP_011533048.1:n.*116G>T
|
|
XM_005266021.4:c.*116G>T
|
XP_005266078.1:n.*116G>T
|
|
XM_011534746.2:c.*116G>T
|
XP_011533048.1:n.*116G>T
|
|
NM_018941.4:c.*116G>T
MANE Select
|
NP_061764.2:n.*116G>T
|
|