ENST00000576204.6:n.771C>T
|
|
|
ENST00000622290.5:c.*80C>T
|
ENSP00000483331.2:n.*80C>T
|
|
ENST00000205557.12:c.3908C>T
MANE Select
|
ENSP00000205557.7:p.Ala1303Val
|
|
ENST00000640696.1:c.722C>T
|
ENSP00000492197.1:p.Ala241Val
|
|
ENST00000205557.11:c.3908C>T
|
ENSP00000205557.7:p.Ala1303Val
|
|
ENST00000456970.6:c.3533C>T
|
ENSP00000405002.2:n.3533C>T
|
|
ENST00000576204.5:n.771C>T
|
|
|
ENST00000622290.4:c.*1117C>T
|
ENSP00000483331.1:n.*1117C>T
|
|
NM_001171.5:c.3908C>T
|
NP_001162.4:p.Ala1303Val
|
|
XM_011522479.1:c.3875C>T
|
XP_011520781.1:p.Ala1292Val
|
|
XM_011522480.1:c.3566C>T
|
XP_011520782.1:p.Ala1189Val
|
|
XM_011522481.1:c.3566C>T
|
XP_011520783.1:p.Ala1189Val
|
|
XR_932836.1:n.4206C>T
|
|
|
XR_932837.1:n.3944C>T
|
|
|
XR_932838.1:n.4007C>T
|
|
|
XR_933134.1:n.539-4775G>A
|
|
|
NM_001351800.1:c.3566C>T
|
NP_001338729.1:p.Ala1189Val
|
|
NR_147784.1:n.3570C>T
|
|
|
XM_011522479.2:c.3875C>T
|
XP_011520781.1:p.Ala1292Val
|
|
XM_011522481.3:c.3566C>T
|
XP_011520783.1:p.Ala1189Val
|
|
XM_017023212.1:c.3740C>T
|
XP_016878701.1:p.Ala1247Val
|
|
XM_024450261.1:c.3944C>T
|
XP_024306029.1:p.Ala1315Val
|
|
XR_932836.2:n.4152C>T
|
|
|
XR_932837.3:n.3889C>T
|
|
|
XR_932838.3:n.3952C>T
|
|
|
NM_001171.6:c.3908C>T
MANE Select
|
NP_001162.5:p.Ala1303Val
|
|