|
NM_000062.3:c.1269T>A
MANE Select
|
NP_000053.2:p.Tyr423Ter
|
|
ENST00000278407.9:c.1269T>A
MANE Select
|
ENSP00000278407.4:p.Tyr423Ter
|
|
NM_000062.2:c.1269T>A , LRG_105t1:c.1269T>A
|
NP_000053.2:p.Tyr423Ter
|
|
NM_001032295.1:c.1269T>A
|
NP_001027466.1:p.Tyr423Ter
|
|
NM_001032295.2:c.1269T>A
|
NP_001027466.1:p.Tyr423Ter
|
|
ENST00000278407.8:c.1269T>A
|
ENSP00000278407.4:p.Tyr423Ter
|
|
ENST00000340687.10:c.1158T>A
|
ENSP00000341861.6:p.Tyr386Ter
|
|
ENST00000378323.8:c.1284T>A
|
ENSP00000367574.4:p.Tyr428Ter
|
|
ENST00000378324.6:c.1113T>A
|
ENSP00000367575.2:p.Tyr371Ter
|
|
ENST00000403558.1:c.1398T>A
|
ENSP00000384420.1:p.Tyr466Ter
|
|
ENST00000528996.1:c.470T>A
|
ENSP00000431226.1:n.470T>A
|
|
ENST00000528996.2:c.*166T>A
|
ENSP00000431226.2:n.*166T>A
|
|
ENST00000530113.1:n.726T>A
|
|
|
ENST00000531133.5:c.770T>A
|
ENSP00000435431.1:n.770T>A
|
|
ENST00000531605.2:c.*1045T>A
|
ENSP00000503752.1:n.*1045T>A
|
|
ENST00000531797.5:c.*294T>A
|
ENSP00000432554.1:n.*294T>A
|
|
ENST00000619430.1:c.400T>A
|
ENSP00000478572.1:p.Ter134Arg
|
|
ENST00000619430.2:c.1065T>A
|
ENSP00000478572.2:p.Tyr355Ter
|
|
ENST00000676670.1:c.1269T>A
|
ENSP00000504807.1:p.Tyr423Ter
|
|
ENST00000676741.1:n.2351T>A
|
|
|
ENST00000677624.1:c.*689T>A
|
ENSP00000503979.1:n.*689T>A
|
|
ENST00000677625.1:c.1215T>A
|
ENSP00000502857.1:p.Tyr405Ter
|
|
ENST00000677856.1:n.1522T>A
|
|
|
ENST00000677915.1:c.*166T>A
|
ENSP00000503118.1:n.*166T>A
|
|
ENST00000678533.1:c.*823T>A
|
ENSP00000503873.1:n.*823T>A
|
|
ENST00000678592.1:c.*209T>A
|
ENSP00000504424.1:n.*209T>A
|