ENST00000439741.4:c.1632G>A
MANE Select
|
ENSP00000391668.2:p.Trp544Ter
|
|
ENST00000369140.7:c.1416G>A
|
ENSP00000358136.3:p.Trp472Ter
|
|
ENST00000439741.2:c.1632G>A
|
ENSP00000391668.2:p.Trp544Ter
|
|
ENST00000466496.5:n.952G>A
|
|
|
ENST00000482025.5:n.1858G>A
|
|
|
ENST00000482343.5:n.1456G>A
|
|
|
ENST00000490310.1:n.764G>A
|
|
|
ENST00000492824.5:n.2052G>A
|
|
|
ENST00000495054.1:n.675G>A
|
|
|
NM_001145862.1:c.1632G>A
|
NP_001139334.1:p.Trp544Ter
|
|
NM_181873.3:c.1416G>A
|
NP_870988.2:p.Trp472Ter
|
|
XM_006711135.1:c.1524G>A
|
XP_006711198.1:p.Trp508Ter
|
|
XM_006711136.2:c.1416G>A
|
XP_006711199.1:p.Trp472Ter
|
|
XM_006711137.1:c.1416G>A
|
XP_006711200.1:p.Trp472Ter
|
|
XM_011509098.1:c.1548G>A
|
XP_011507400.1:p.Trp516Ter
|
|
XM_011509099.1:c.*590G>A
|
XP_011507401.1:n.*590G>A
|
|
XR_426759.2:n.1823G>A
|
|
|
XR_426760.2:n.1729G>A
|
|
|
XM_011509099.3:c.*590G>A
|
XP_011507401.1:n.*590G>A
|
|
XM_024452577.1:c.1548G>A
|
XP_024308345.1:p.Trp516Ter
|
|
XM_024452578.1:c.1524G>A
|
XP_024308346.1:p.Trp508Ter
|
|
XR_002959043.1:n.1845G>A
|
|
|
XR_002959062.1:n.1961G>A
|
|
|
XR_002959066.1:n.1663G>A
|
|
|
XR_002959067.1:n.3182G>A
|
|
|
XR_426760.4:n.1751G>A
|
|
|
NM_001145862.2:c.1632G>A
MANE Select
|
NP_001139334.1:p.Trp544Ter
|
|