ENST00000234071.8:c.995A>G
MANE Select
|
ENSP00000234071.4:p.Gln332Arg
|
|
ENST00000234071.7:c.995A>G
|
ENSP00000234071.3:p.Gln332Arg
|
|
ENST00000402125.2:c.319A>G
|
|
|
ENST00000409048.1:c.1097A>G
|
ENSP00000386679.1:p.Gln366Arg
|
|
NM_000312.3:c.995A>G , LRG_599t1:c.995A>G
|
NP_000303.1:p.Gln332Arg
|
|
XM_005263715.3:c.1178A>G
|
XP_005263772.1:p.Gln393Arg
|
|
XM_005263716.3:c.1160A>G
|
XP_005263773.1:p.Gln387Arg
|
|
XM_005263717.3:c.1058A>G
|
XP_005263774.1:p.Gln353Arg
|
|
XR_923313.1:n.1332-291T>C
|
|
|
XM_005263717.4:c.1058A>G
|
XP_005263774.1:p.Gln353Arg
|
|
XM_017004505.1:c.1238A>G
|
XP_016859994.1:p.Gln413Arg
|
|
XM_024453002.1:c.1340A>G
|
XP_024308770.1:p.Gln447Arg
|
|
XM_024453003.1:c.1280A>G
|
XP_024308771.1:p.Gln427Arg
|
|
XM_024453004.1:c.1178A>G
|
XP_024308772.1:p.Gln393Arg
|
|
XM_024453005.1:c.1160A>G
|
XP_024308773.1:p.Gln387Arg
|
|
XM_024453006.1:c.1097A>G
|
XP_024308774.1:p.Gln366Arg
|
|
XR_001739705.1:n.3607-291T>C
|
|
|
XR_923313.2:n.4043-291T>C
|
|
|
NM_000312.4:c.995A>G
MANE Select
|
NP_000303.1:p.Gln332Arg
|
|
NM_001375602.1:c.1178A>G
|
NP_001362531.1:p.Gln393Arg
|
|
NM_001375603.1:c.1160A>G
|
NP_001362532.1:p.Gln387Arg
|
|
NM_001375604.1:c.1058A>G
|
NP_001362533.1:p.Gln353Arg
|
|
NM_001375605.1:c.1097A>G
|
NP_001362534.1:p.Gln366Arg
|
|
NM_001375606.1:c.1163A>G
|
NP_001362535.1:p.Gln388Arg
|
|
NM_001375607.1:c.1181A>G
|
NP_001362536.1:p.Gln394Arg
|
|
NM_001375608.1:c.938A>G
|
NP_001362537.1:p.Gln313Arg
|
|
NM_001375609.1:c.971A>G
|
NP_001362538.1:p.Gln324Arg
|
|
NM_001375610.1:c.989A>G
|
NP_001362539.1:p.Gln330Arg
|
|
NM_001375611.1:c.995A>G
|
NP_001362540.1:p.Gln332Arg
|
|
NM_001375613.1:c.995A>G
|
NP_001362542.1:p.Gln332Arg
|
|