ENST00000622290.5:c.*346C>G
|
ENSP00000483331.2:n.*346C>G
|
|
ENST00000205557.12:c.4174C>G
MANE Select
|
ENSP00000205557.7:p.Gln1392Glu
|
|
ENST00000640696.1:c.988C>G
|
ENSP00000492197.1:p.Gln330Glu
|
|
ENST00000205557.11:c.4174C>G
|
ENSP00000205557.7:p.Gln1392Glu
|
|
ENST00000456970.6:c.3799C>G
|
ENSP00000405002.2:n.3799C>G
|
|
ENST00000576204.5:n.1037C>G
|
|
|
ENST00000622290.4:c.*1383C>G
|
ENSP00000483331.1:n.*1383C>G
|
|
NM_001171.5:c.4174C>G
|
NP_001162.4:p.Gln1392Glu
|
|
XM_011522479.1:c.4141C>G
|
XP_011520781.1:p.Gln1381Glu
|
|
XM_011522480.1:c.3832C>G
|
XP_011520782.1:p.Gln1278Glu
|
|
XM_011522481.1:c.3832C>G
|
XP_011520783.1:p.Gln1278Glu
|
|
XR_933134.1:n.539-5119G>C
|
|
|
NM_001351800.1:c.3832C>G
|
NP_001338729.1:p.Gln1278Glu
|
|
NR_147784.1:n.3836C>G
|
|
|
XM_011522479.2:c.4141C>G
|
XP_011520781.1:p.Gln1381Glu
|
|
XM_011522481.3:c.3832C>G
|
XP_011520783.1:p.Gln1278Glu
|
|
XM_017023212.1:c.4006C>G
|
XP_016878701.1:p.Gln1336Glu
|
|
XM_024450261.1:c.4210C>G
|
XP_024306029.1:p.Gln1404Glu
|
|
NM_001171.6:c.4174C>G
MANE Select
|
NP_001162.5:p.Gln1392Glu
|
|