ENST00000255078.8:c.1953T>G
MANE Select
|
ENSP00000255078.4:p.Tyr651Ter
|
|
ENST00000674675.1:c.197T>G
|
|
|
ENST00000674878.1:c.197T>G
|
|
|
ENST00000674955.1:c.*670T>G
|
ENSP00000502463.1:n.*670T>G
|
|
ENST00000675118.1:c.1441T>G
|
|
|
ENST00000675389.1:n.228T>G
|
|
|
ENST00000675615.1:c.1953T>G
|
ENSP00000502413.1:p.Tyr651Ter
|
|
ENST00000675648.1:n.1328T>G
|
|
|
ENST00000675916.1:c.197T>G
|
|
|
ENST00000676173.1:n.2698T>G
|
|
|
ENST00000676182.1:c.384T>G
|
|
|
ENST00000676228.1:c.*1276T>G
|
ENSP00000502375.1:n.*1276T>G
|
|
ENST00000255078.7:c.1953T>G
|
ENSP00000255078.3:p.Tyr651Ter
|
|
ENST00000539064.5:n.1712T>G
|
|
|
ENST00000543739.5:n.946T>G
|
|
|
ENST00000545475.1:n.549T>G
|
|
|
NM_002180.2:c.1953T>G , LRG_250t1:c.1953T>G
|
NP_002171.2:p.Tyr651Ter
|
|
XM_005273974.2:c.942T>G
|
XP_005274031.1:p.Tyr314Ter
|
|
XM_005273975.2:c.825T>G
|
XP_005274032.1:p.Tyr275Ter
|
|
XM_011544994.1:c.720T>G
|
XP_011543296.1:p.Tyr240Ter
|
|
XR_949903.1:n.2055T>G
|
|
|
XM_005273975.3:c.825T>G
|
XP_005274032.1:p.Tyr275Ter
|
|
XM_017017669.2:c.942T>G
|
XP_016873158.1:p.Tyr314Ter
|
|
XM_017017670.2:c.942T>G
|
XP_016873159.1:p.Tyr314Ter
|
|
XR_949903.3:n.2051T>G
|
|
|
NM_002180.3:c.1953T>G
MANE Select
|
NP_002171.2:p.Tyr651Ter
|
|