ENST00000622290.5:c.*655A>G
|
ENSP00000483331.2:n.*655A>G
|
|
ENST00000205557.12:c.4483A>G
MANE Select
|
ENSP00000205557.7:p.Arg1495Gly
|
|
ENST00000640696.1:c.1297A>G
|
ENSP00000492197.1:p.Arg433Gly
|
|
ENST00000205557.11:c.4483A>G
|
ENSP00000205557.7:p.Arg1495Gly
|
|
ENST00000456970.6:c.4108A>G
|
ENSP00000405002.2:n.4108A>G
|
|
ENST00000576204.5:n.1346A>G
|
|
|
ENST00000622290.4:c.*1692A>G
|
ENSP00000483331.1:n.*1692A>G
|
|
NM_001171.5:c.4483A>G
|
NP_001162.4:p.Arg1495Gly
|
|
XM_011522479.1:c.4450A>G
|
XP_011520781.1:p.Arg1484Gly
|
|
XM_011522480.1:c.4141A>G
|
XP_011520782.1:p.Arg1381Gly
|
|
XM_011522481.1:c.4141A>G
|
XP_011520783.1:p.Arg1381Gly
|
|
XR_933134.1:n.538+5872T>C
|
|
|
NM_001351800.1:c.4141A>G
|
NP_001338729.1:p.Arg1381Gly
|
|
NR_147784.1:n.4145A>G
|
|
|
XM_011522479.2:c.4450A>G
|
XP_011520781.1:p.Arg1484Gly
|
|
XM_011522481.3:c.4141A>G
|
XP_011520783.1:p.Arg1381Gly
|
|
XM_017023212.1:c.4315A>G
|
XP_016878701.1:p.Arg1439Gly
|
|
XM_024450261.1:c.4519A>G
|
XP_024306029.1:p.Arg1507Gly
|
|
NM_001171.6:c.4483A>G
MANE Select
|
NP_001162.5:p.Arg1495Gly
|
|