ENST00000622290.5:c.*341A>G
|
ENSP00000483331.2:n.*341A>G
|
|
ENST00000205557.12:c.4169A>G
MANE Select
|
ENSP00000205557.7:p.Gln1390Arg
|
|
ENST00000640696.1:c.983A>G
|
ENSP00000492197.1:p.Gln328Arg
|
|
ENST00000205557.11:c.4169A>G
|
ENSP00000205557.7:p.Gln1390Arg
|
|
ENST00000456970.6:c.3794A>G
|
ENSP00000405002.2:n.3794A>G
|
|
ENST00000576204.5:n.1032A>G
|
|
|
ENST00000622290.4:c.*1378A>G
|
ENSP00000483331.1:n.*1378A>G
|
|
NM_001171.5:c.4169A>G
|
NP_001162.4:p.Gln1390Arg
|
|
XM_011522479.1:c.4136A>G
|
XP_011520781.1:p.Gln1379Arg
|
|
XM_011522480.1:c.3827A>G
|
XP_011520782.1:p.Gln1276Arg
|
|
XM_011522481.1:c.3827A>G
|
XP_011520783.1:p.Gln1276Arg
|
|
XR_933134.1:n.539-5114T>C
|
|
|
NM_001351800.1:c.3827A>G
|
NP_001338729.1:p.Gln1276Arg
|
|
NR_147784.1:n.3831A>G
|
|
|
XM_011522479.2:c.4136A>G
|
XP_011520781.1:p.Gln1379Arg
|
|
XM_011522481.3:c.3827A>G
|
XP_011520783.1:p.Gln1276Arg
|
|
XM_017023212.1:c.4001A>G
|
XP_016878701.1:p.Gln1334Arg
|
|
XM_024450261.1:c.4205A>G
|
XP_024306029.1:p.Gln1402Arg
|
|
NM_001171.6:c.4169A>G
MANE Select
|
NP_001162.5:p.Gln1390Arg
|
|