ENST00000576204.6:n.854G>T
|
|
|
ENST00000622290.5:c.*163G>T
|
ENSP00000483331.2:n.*163G>T
|
|
ENST00000205557.12:c.3991G>T
MANE Select
|
ENSP00000205557.7:p.Ala1331Ser
|
|
ENST00000640696.1:c.805G>T
|
ENSP00000492197.1:p.Ala269Ser
|
|
ENST00000205557.11:c.3991G>T
|
ENSP00000205557.7:p.Ala1331Ser
|
|
ENST00000456970.6:c.3616G>T
|
ENSP00000405002.2:n.3616G>T
|
|
ENST00000576204.5:n.854G>T
|
|
|
ENST00000622290.4:c.*1200G>T
|
ENSP00000483331.1:n.*1200G>T
|
|
NM_001171.5:c.3991G>T
|
NP_001162.4:p.Ala1331Ser
|
|
XM_011522479.1:c.3958G>T
|
XP_011520781.1:p.Ala1320Ser
|
|
XM_011522480.1:c.3649G>T
|
XP_011520782.1:p.Ala1217Ser
|
|
XM_011522481.1:c.3649G>T
|
XP_011520783.1:p.Ala1217Ser
|
|
XR_933134.1:n.539-4858C>A
|
|
|
NM_001351800.1:c.3649G>T
|
NP_001338729.1:p.Ala1217Ser
|
|
NR_147784.1:n.3653G>T
|
|
|
XM_011522479.2:c.3958G>T
|
XP_011520781.1:p.Ala1320Ser
|
|
XM_011522481.3:c.3649G>T
|
XP_011520783.1:p.Ala1217Ser
|
|
XM_017023212.1:c.3823G>T
|
XP_016878701.1:p.Ala1275Ser
|
|
XM_024450261.1:c.4027G>T
|
XP_024306029.1:p.Ala1343Ser
|
|
NM_001171.6:c.3991G>T
MANE Select
|
NP_001162.5:p.Ala1331Ser
|
|