ENST00000262367.10:c.4416G>A
MANE Select
|
ENSP00000262367.5:p.Trp1472Ter
|
|
ENST00000262367.9:c.4416G>A
|
ENSP00000262367.5:p.Trp1472Ter
|
|
ENST00000382070.7:c.4302G>A
|
ENSP00000371502.3:p.Trp1434Ter
|
|
ENST00000570939.2:c.3051G>A
|
ENSP00000461002.2:p.Trp1017Ter
|
|
ENST00000571763.5:n.206G>A
|
|
|
ENST00000574740.1:n.237G>A
|
|
|
ENST00000576720.1:n.3239G>A
|
|
|
NM_001079846.1:c.4302G>A
|
NP_001073315.1:p.Trp1434Ter
|
|
NM_004380.2:c.4416G>A
|
NP_004371.2:p.Trp1472Ter
|
|
XM_005255124.3:c.4371G>A
|
XP_005255181.1:p.Trp1457Ter
|
|
XM_005255125.3:c.3999G>A
|
XP_005255182.1:p.Trp1333Ter
|
|
XM_006720848.2:c.4155G>A
|
XP_006720911.1:p.Trp1385Ter
|
|
XM_011522380.1:c.4362G>A
|
XP_011520682.1:p.Trp1454Ter
|
|
XM_011522381.1:c.3663G>A
|
XP_011520683.1:p.Trp1221Ter
|
|
XM_005255124.4:c.4371G>A
|
XP_005255181.1:p.Trp1457Ter
|
|
XM_005255125.4:c.3999G>A
|
XP_005255182.1:p.Trp1333Ter
|
|
XM_006720848.3:c.4155G>A
|
XP_006720911.1:p.Trp1385Ter
|
|
XM_011522381.2:c.3663G>A
|
XP_011520683.1:p.Trp1221Ter
|
|
XM_017022944.1:c.4410G>A
|
XP_016878433.1:p.Trp1470Ter
|
|
NM_004380.3:c.4416G>A
MANE Select
|
NP_004371.2:p.Trp1472Ter
|
|