ENST00000298139.7:c.4220T>A
MANE Select
|
ENSP00000298139.5:p.Leu1407Ter
|
|
ENST00000650667.1:c.*3834T>A
|
ENSP00000498593.1:n.*3834T>A
|
|
ENST00000651946.1:n.444T>A
|
|
|
ENST00000298139.5:c.4220T>A
|
ENSP00000298139.5:p.Leu1407Ter
|
|
ENST00000521620.5:n.2853T>A
|
|
|
NM_000553.4:c.4220T>A , LRG_524t1:c.4220T>A
|
NP_000544.2:p.Leu1407Ter
|
|
XM_011544639.1:c.4139T>A
|
XP_011542941.1:p.Leu1380Ter
|
|
XM_011544640.1:c.2621T>A
|
XP_011542942.1:p.Leu874Ter
|
|
XR_949643.1:n.88-1705A>T
|
|
|
XR_949644.1:n.88-1705A>T
|
|
|
XR_949645.1:n.88-1705A>T
|
|
|
XR_949646.1:n.88-1705A>T
|
|
|
XR_949647.1:n.701-1705A>T
|
|
|
XR_949648.1:n.603-1705A>T
|
|
|
NM_000553.5:c.4220T>A
|
NP_000544.2:p.Leu1407Ter
|
|
XM_011544639.3:c.4139T>A
|
XP_011542941.1:p.Leu1380Ter
|
|
XM_024447265.1:c.4010T>A
|
XP_024303033.1:p.Leu1337Ter
|
|
NM_000553.6:c.4220T>A
MANE Select
|
NP_000544.2:p.Leu1407Ter
|
|