ENST00000576204.6:n.775G>T
|
|
|
ENST00000622290.5:c.*84G>T
|
ENSP00000483331.2:n.*84G>T
|
|
ENST00000205557.12:c.3912G>T
MANE Select
|
ENSP00000205557.7:p.Gly1304=
|
|
ENST00000640696.1:c.726G>T
|
ENSP00000492197.1:p.Gly242=
|
|
ENST00000205557.11:c.3912G>T
|
ENSP00000205557.7:p.Gly1304=
|
|
ENST00000456970.6:c.3537G>T
|
ENSP00000405002.2:n.3537G>T
|
|
ENST00000576204.5:n.775G>T
|
|
|
ENST00000622290.4:c.*1121G>T
|
ENSP00000483331.1:n.*1121G>T
|
|
NM_001171.5:c.3912G>T
|
NP_001162.4:p.Gly1304=
|
|
XM_011522479.1:c.3879G>T
|
XP_011520781.1:p.Gly1293=
|
|
XM_011522480.1:c.3570G>T
|
XP_011520782.1:p.Gly1190=
|
|
XM_011522481.1:c.3570G>T
|
XP_011520783.1:p.Gly1190=
|
|
XR_932836.1:n.4210G>T
|
|
|
XR_932837.1:n.3948G>T
|
|
|
XR_932838.1:n.4011G>T
|
|
|
XR_933134.1:n.539-4779C>A
|
|
|
NM_001351800.1:c.3570G>T
|
NP_001338729.1:p.Gly1190=
|
|
NR_147784.1:n.3574G>T
|
|
|
XM_011522479.2:c.3879G>T
|
XP_011520781.1:p.Gly1293=
|
|
XM_011522481.3:c.3570G>T
|
XP_011520783.1:p.Gly1190=
|
|
XM_017023212.1:c.3744G>T
|
XP_016878701.1:p.Gly1248=
|
|
XM_024450261.1:c.3948G>T
|
XP_024306029.1:p.Gly1316=
|
|
XR_932836.2:n.4156G>T
|
|
|
XR_932837.3:n.3893G>T
|
|
|
XR_932838.3:n.3956G>T
|
|
|
NM_001171.6:c.3912G>T
MANE Select
|
NP_001162.5:p.Gly1304=
|
|