ENST00000622290.5:c.*1081G>A
|
ENSP00000483331.2:n.*1081G>A
|
|
ENST00000205557.12:c.*397G>A
MANE Select
|
ENSP00000205557.7:n.*397G>A
|
|
ENST00000640696.1:c.1723G>A
|
ENSP00000492197.1:n.1723G>A
|
|
ENST00000205557.11:c.*397G>A
|
ENSP00000205557.7:n.*397G>A
|
|
ENST00000576204.5:n.1772G>A
|
|
|
ENST00000622290.4:c.*2118G>A
|
ENSP00000483331.1:n.*2118G>A
|
|
NM_001171.5:c.*397G>A
|
NP_001162.4:n.*397G>A
|
|
XM_011522479.1:c.*397G>A
|
XP_011520781.1:n.*397G>A
|
|
XM_011522480.1:c.*397G>A
|
XP_011520782.1:n.*397G>A
|
|
XM_011522481.1:c.*397G>A
|
XP_011520783.1:n.*397G>A
|
|
XR_933134.1:n.538+5446C>T
|
|
|
NM_001351800.1:c.*397G>A
|
NP_001338729.1:n.*397G>A
|
|
NR_147784.1:n.4571G>A
|
|
|
XM_011522479.2:c.*397G>A
|
XP_011520781.1:n.*397G>A
|
|
XM_011522481.3:c.*397G>A
|
XP_011520783.1:n.*397G>A
|
|
XM_017023212.1:c.*397G>A
|
XP_016878701.1:n.*397G>A
|
|
XM_024450261.1:c.*397G>A
|
XP_024306029.1:n.*397G>A
|
|
NM_001171.6:c.*397G>A
MANE Select
|
NP_001162.5:n.*397G>A
|
|