ENST00000576204.6:n.846T>C
|
|
|
ENST00000622290.5:c.*155T>C
|
ENSP00000483331.2:n.*155T>C
|
|
ENST00000205557.12:c.3983T>C
MANE Select
|
ENSP00000205557.7:p.Val1328Ala
|
|
ENST00000640696.1:c.797T>C
|
ENSP00000492197.1:p.Val266Ala
|
|
ENST00000205557.11:c.3983T>C
|
ENSP00000205557.7:p.Val1328Ala
|
|
ENST00000456970.6:c.3608T>C
|
ENSP00000405002.2:n.3608T>C
|
|
ENST00000576204.5:n.846T>C
|
|
|
ENST00000622290.4:c.*1192T>C
|
ENSP00000483331.1:n.*1192T>C
|
|
NM_001171.5:c.3983T>C
|
NP_001162.4:p.Val1328Ala
|
|
XM_011522479.1:c.3950T>C
|
XP_011520781.1:p.Val1317Ala
|
|
XM_011522480.1:c.3641T>C
|
XP_011520782.1:p.Val1214Ala
|
|
XM_011522481.1:c.3641T>C
|
XP_011520783.1:p.Val1214Ala
|
|
XR_933134.1:n.539-4850A>G
|
|
|
NM_001351800.1:c.3641T>C
|
NP_001338729.1:p.Val1214Ala
|
|
NR_147784.1:n.3645T>C
|
|
|
XM_011522479.2:c.3950T>C
|
XP_011520781.1:p.Val1317Ala
|
|
XM_011522481.3:c.3641T>C
|
XP_011520783.1:p.Val1214Ala
|
|
XM_017023212.1:c.3815T>C
|
XP_016878701.1:p.Val1272Ala
|
|
XM_024450261.1:c.4019T>C
|
XP_024306029.1:p.Val1340Ala
|
|
NM_001171.6:c.3983T>C
MANE Select
|
NP_001162.5:p.Val1328Ala
|
|