ENST00000576204.6:n.812G>T
|
|
|
ENST00000622290.5:c.*121G>T
|
ENSP00000483331.2:n.*121G>T
|
|
ENST00000205557.12:c.3949G>T
MANE Select
|
ENSP00000205557.7:p.Glu1317Ter
|
|
ENST00000640696.1:c.763G>T
|
ENSP00000492197.1:p.Glu255Ter
|
|
ENST00000205557.11:c.3949G>T
|
ENSP00000205557.7:p.Glu1317Ter
|
|
ENST00000456970.6:c.3574G>T
|
ENSP00000405002.2:n.3574G>T
|
|
ENST00000576204.5:n.812G>T
|
|
|
ENST00000622290.4:c.*1158G>T
|
ENSP00000483331.1:n.*1158G>T
|
|
NM_001171.5:c.3949G>T
|
NP_001162.4:p.Glu1317Ter
|
|
XM_011522479.1:c.3916G>T
|
XP_011520781.1:p.Glu1306Ter
|
|
XM_011522480.1:c.3607G>T
|
XP_011520782.1:p.Glu1203Ter
|
|
XM_011522481.1:c.3607G>T
|
XP_011520783.1:p.Glu1203Ter
|
|
XR_932836.1:n.4247G>T
|
|
|
XR_932837.1:n.3985G>T
|
|
|
XR_932838.1:n.4048G>T
|
|
|
XR_933134.1:n.539-4816C>A
|
|
|
NM_001351800.1:c.3607G>T
|
NP_001338729.1:p.Glu1203Ter
|
|
NR_147784.1:n.3611G>T
|
|
|
XM_011522479.2:c.3916G>T
|
XP_011520781.1:p.Glu1306Ter
|
|
XM_011522481.3:c.3607G>T
|
XP_011520783.1:p.Glu1203Ter
|
|
XM_017023212.1:c.3781G>T
|
XP_016878701.1:p.Glu1261Ter
|
|
XM_024450261.1:c.3985G>T
|
XP_024306029.1:p.Glu1329Ter
|
|
XR_932837.3:n.3930G>T
|
|
|
NM_001171.6:c.3949G>T
MANE Select
|
NP_001162.5:p.Glu1317Ter
|
|