ENST00000622290.5:c.*867C>A
|
ENSP00000483331.2:n.*867C>A
|
|
ENST00000205557.12:c.*183C>A
MANE Select
|
ENSP00000205557.7:n.*183C>A
|
|
ENST00000640696.1:c.1509C>A
|
ENSP00000492197.1:n.1509C>A
|
|
ENST00000205557.11:c.*183C>A
|
ENSP00000205557.7:n.*183C>A
|
|
ENST00000576204.5:n.1558C>A
|
|
|
ENST00000622290.4:c.*1904C>A
|
ENSP00000483331.1:n.*1904C>A
|
|
NM_001171.5:c.*183C>A
|
NP_001162.4:n.*183C>A
|
|
XM_011522479.1:c.*183C>A
|
XP_011520781.1:n.*183C>A
|
|
XM_011522480.1:c.*183C>A
|
XP_011520782.1:n.*183C>A
|
|
XM_011522481.1:c.*183C>A
|
XP_011520783.1:n.*183C>A
|
|
XR_933134.1:n.538+5660G>T
|
|
|
NM_001351800.1:c.*183C>A
|
NP_001338729.1:n.*183C>A
|
|
NR_147784.1:n.4357C>A
|
|
|
XM_011522479.2:c.*183C>A
|
XP_011520781.1:n.*183C>A
|
|
XM_011522481.3:c.*183C>A
|
XP_011520783.1:n.*183C>A
|
|
XM_017023212.1:c.*183C>A
|
XP_016878701.1:n.*183C>A
|
|
XM_024450261.1:c.*183C>A
|
XP_024306029.1:n.*183C>A
|
|
NM_001171.6:c.*183C>A
MANE Select
|
NP_001162.5:n.*183C>A
|
|