ENST00000278407.9:c.*6G>T
MANE Select
|
ENSP00000278407.4:n.*6G>T
|
|
ENST00000528996.2:c.*406G>T
|
ENSP00000431226.2:n.*406G>T
|
|
ENST00000531605.2:c.*1285G>T
|
ENSP00000503752.1:n.*1285G>T
|
|
ENST00000619430.2:c.*6G>T
|
ENSP00000478572.2:n.*6G>T
|
|
ENST00000676670.1:c.*6G>T
|
ENSP00000504807.1:n.*6G>T
|
|
ENST00000676741.1:n.2591G>T
|
|
|
ENST00000677624.1:c.*929G>T
|
ENSP00000503979.1:n.*929G>T
|
|
ENST00000677625.1:c.*6G>T
|
ENSP00000502857.1:n.*6G>T
|
|
ENST00000677856.1:n.1762G>T
|
|
|
ENST00000677915.1:c.*406G>T
|
ENSP00000503118.1:n.*406G>T
|
|
ENST00000678533.1:c.*1063G>T
|
ENSP00000503873.1:n.*1063G>T
|
|
ENST00000678592.1:c.*449G>T
|
ENSP00000504424.1:n.*449G>T
|
|
ENST00000278407.8:c.*6G>T
|
ENSP00000278407.4:n.*6G>T
|
|
ENST00000340687.10:c.*6G>T
|
ENSP00000341861.6:n.*6G>T
|
|
ENST00000378323.8:c.*6G>T
|
ENSP00000367574.4:n.*6G>T
|
|
ENST00000378324.6:c.*6G>T
|
ENSP00000367575.2:n.*6G>T
|
|
ENST00000403558.1:c.*6G>T
|
ENSP00000384420.1:n.*6G>T
|
|
ENST00000528996.1:c.710G>T
|
ENSP00000431226.1:n.710G>T
|
|
ENST00000531797.5:c.*534G>T
|
ENSP00000432554.1:n.*534G>T
|
|
NM_000062.2:c.*6G>T , LRG_105t1:c.*6G>T
|
NP_000053.2:n.*6G>T
|
|
NM_001032295.1:c.*6G>T
|
NP_001027466.1:n.*6G>T
|
|
NM_000062.3:c.*6G>T
MANE Select
|
NP_000053.2:n.*6G>T
|
|
NM_001032295.2:c.*6G>T
|
NP_001027466.1:n.*6G>T
|
|