ENST00000622290.5:c.3667T>G
|
ENSP00000483331.2:p.Trp1223Gly
|
|
ENST00000205557.12:c.3667T>G
MANE Select
|
ENSP00000205557.7:p.Trp1223Gly
|
|
ENST00000640696.1:c.481T>G
|
ENSP00000492197.1:p.Trp161Gly
|
|
ENST00000205557.11:c.3667T>G
|
ENSP00000205557.7:p.Trp1223Gly
|
|
ENST00000456970.6:c.3292T>G
|
ENSP00000405002.2:n.3292T>G
|
|
ENST00000622290.4:c.*876T>G
|
ENSP00000483331.1:n.*876T>G
|
|
NM_001171.5:c.3667T>G
|
NP_001162.4:p.Trp1223Gly
|
|
XM_011522479.1:c.3634T>G
|
XP_011520781.1:p.Trp1212Gly
|
|
XM_011522480.1:c.3325T>G
|
XP_011520782.1:p.Trp1109Gly
|
|
XM_011522481.1:c.3325T>G
|
XP_011520783.1:p.Trp1109Gly
|
|
XR_932836.1:n.3902T>G
|
|
|
XR_932837.1:n.3703T>G
|
|
|
XR_932838.1:n.3703T>G
|
|
|
XR_933134.1:n.539-231A>C
|
|
|
NM_001351800.1:c.3325T>G
|
NP_001338729.1:p.Trp1109Gly
|
|
NR_147784.1:n.3329T>G
|
|
|
XM_011522479.2:c.3634T>G
|
XP_011520781.1:p.Trp1212Gly
|
|
XM_011522481.3:c.3325T>G
|
XP_011520783.1:p.Trp1109Gly
|
|
XM_017023212.1:c.3499T>G
|
XP_016878701.1:p.Trp1167Gly
|
|
XM_024450261.1:c.3703T>G
|
XP_024306029.1:p.Trp1235Gly
|
|
XR_932836.2:n.3848T>G
|
|
|
XR_932837.3:n.3648T>G
|
|
|
XR_932838.3:n.3648T>G
|
|
|
NM_001171.6:c.3667T>G
MANE Select
|
NP_001162.5:p.Trp1223Gly
|
|