ENST00000576204.6:n.828G>T
|
|
|
ENST00000622290.5:c.*137G>T
|
ENSP00000483331.2:n.*137G>T
|
|
ENST00000205557.12:c.3965G>T
MANE Select
|
ENSP00000205557.7:p.Gly1322Val
|
|
ENST00000640696.1:c.779G>T
|
ENSP00000492197.1:p.Gly260Val
|
|
ENST00000205557.11:c.3965G>T
|
ENSP00000205557.7:p.Gly1322Val
|
|
ENST00000456970.6:c.3590G>T
|
ENSP00000405002.2:n.3590G>T
|
|
ENST00000576204.5:n.828G>T
|
|
|
ENST00000622290.4:c.*1174G>T
|
ENSP00000483331.1:n.*1174G>T
|
|
NM_001171.5:c.3965G>T
|
NP_001162.4:p.Gly1322Val
|
|
XM_011522479.1:c.3932G>T
|
XP_011520781.1:p.Gly1311Val
|
|
XM_011522480.1:c.3623G>T
|
XP_011520782.1:p.Gly1208Val
|
|
XM_011522481.1:c.3623G>T
|
XP_011520783.1:p.Gly1208Val
|
|
XR_932836.1:n.4263G>T
|
|
|
XR_932837.1:n.4001G>T
|
|
|
XR_932838.1:n.4064G>T
|
|
|
XR_933134.1:n.539-4832C>A
|
|
|
NM_001351800.1:c.3623G>T
|
NP_001338729.1:p.Gly1208Val
|
|
NR_147784.1:n.3627G>T
|
|
|
XM_011522479.2:c.3932G>T
|
XP_011520781.1:p.Gly1311Val
|
|
XM_011522481.3:c.3623G>T
|
XP_011520783.1:p.Gly1208Val
|
|
XM_017023212.1:c.3797G>T
|
XP_016878701.1:p.Gly1266Val
|
|
XM_024450261.1:c.4001G>T
|
XP_024306029.1:p.Gly1334Val
|
|
XR_932837.3:n.3946G>T
|
|
|
NM_001171.6:c.3965G>T
MANE Select
|
NP_001162.5:p.Gly1322Val
|
|