ENST00000622290.5:c.*410C>T
|
ENSP00000483331.2:n.*410C>T
|
|
ENST00000205557.12:c.4238C>T
MANE Select
|
ENSP00000205557.7:p.Ala1413Val
|
|
ENST00000640696.1:c.1052C>T
|
ENSP00000492197.1:p.Ala351Val
|
|
ENST00000205557.11:c.4238C>T
|
ENSP00000205557.7:p.Ala1413Val
|
|
ENST00000456970.6:c.3863C>T
|
ENSP00000405002.2:n.3863C>T
|
|
ENST00000576204.5:n.1101C>T
|
|
|
ENST00000622290.4:c.*1447C>T
|
ENSP00000483331.1:n.*1447C>T
|
|
NM_001171.5:c.4238C>T
|
NP_001162.4:p.Ala1413Val
|
|
XM_011522479.1:c.4205C>T
|
XP_011520781.1:p.Ala1402Val
|
|
XM_011522480.1:c.3896C>T
|
XP_011520782.1:p.Ala1299Val
|
|
XM_011522481.1:c.3896C>T
|
XP_011520783.1:p.Ala1299Val
|
|
XR_933134.1:n.538+6453G>A
|
|
|
NM_001351800.1:c.3896C>T
|
NP_001338729.1:p.Ala1299Val
|
|
NR_147784.1:n.3900C>T
|
|
|
XM_011522479.2:c.4205C>T
|
XP_011520781.1:p.Ala1402Val
|
|
XM_011522481.3:c.3896C>T
|
XP_011520783.1:p.Ala1299Val
|
|
XM_017023212.1:c.4070C>T
|
XP_016878701.1:p.Ala1357Val
|
|
XM_024450261.1:c.4274C>T
|
XP_024306029.1:p.Ala1425Val
|
|
NM_001171.6:c.4238C>T
MANE Select
|
NP_001162.5:p.Ala1413Val
|
|