ENST00000622290.5:c.*338G>A
|
ENSP00000483331.2:n.*338G>A
|
|
ENST00000205557.12:c.4166G>A
MANE Select
|
ENSP00000205557.7:p.Gly1389Asp
|
|
ENST00000640696.1:c.980G>A
|
ENSP00000492197.1:p.Gly327Asp
|
|
ENST00000205557.11:c.4166G>A
|
ENSP00000205557.7:p.Gly1389Asp
|
|
ENST00000456970.6:c.3791G>A
|
ENSP00000405002.2:n.3791G>A
|
|
ENST00000576204.5:n.1029G>A
|
|
|
ENST00000622290.4:c.*1375G>A
|
ENSP00000483331.1:n.*1375G>A
|
|
NM_001171.5:c.4166G>A
|
NP_001162.4:p.Gly1389Asp
|
|
XM_011522479.1:c.4133G>A
|
XP_011520781.1:p.Gly1378Asp
|
|
XM_011522480.1:c.3824G>A
|
XP_011520782.1:p.Gly1275Asp
|
|
XM_011522481.1:c.3824G>A
|
XP_011520783.1:p.Gly1275Asp
|
|
XR_933134.1:n.539-5111C>T
|
|
|
NM_001351800.1:c.3824G>A
|
NP_001338729.1:p.Gly1275Asp
|
|
NR_147784.1:n.3828G>A
|
|
|
XM_011522479.2:c.4133G>A
|
XP_011520781.1:p.Gly1378Asp
|
|
XM_011522481.3:c.3824G>A
|
XP_011520783.1:p.Gly1275Asp
|
|
XM_017023212.1:c.3998G>A
|
XP_016878701.1:p.Gly1333Asp
|
|
XM_024450261.1:c.4202G>A
|
XP_024306029.1:p.Gly1401Asp
|
|
NM_001171.6:c.4166G>A
MANE Select
|
NP_001162.5:p.Gly1389Asp
|
|