ENST00000698727.1:n.1616G>T
|
|
|
ENST00000698728.1:n.2135G>T
|
|
|
ENST00000698729.1:n.3681G>T
|
|
|
ENST00000698730.1:n.3681G>T
|
|
|
ENST00000698731.1:c.2415G>T
|
ENSP00000513898.1:p.Met805Ile
|
|
ENST00000698732.1:c.*1417G>T
|
ENSP00000513899.1:n.*1417G>T
|
|
ENST00000698733.1:c.*1743G>T
|
ENSP00000513900.1:n.*1743G>T
|
|
ENST00000698734.1:c.2556G>T
|
ENSP00000513901.1:p.Met852Ile
|
|
ENST00000698735.1:n.2671G>T
|
|
|
ENST00000698736.1:n.2671G>T
|
|
|
ENST00000698737.1:n.2671G>T
|
|
|
ENST00000698738.1:n.2671G>T
|
|
|
ENST00000698739.1:n.2671G>T
|
|
|
ENST00000372371.8:c.2556G>T
MANE Select
|
ENSP00000361446.3:p.Met852Ile
|
|
ENST00000372371.7:c.2556G>T
|
ENSP00000361446.3:p.Met852Ile
|
|
ENST00000472014.5:n.469+4675G>T
|
|
|
NM_007055.3:c.2556G>T
|
NP_008986.2:p.Met852Ile
|
|
NM_007055.4:c.2556G>T
MANE Select
|
NP_008986.2:p.Met852Ile
|
|