ENST00000645828.1:n.2620G>A
|
|
|
ENST00000651671.1:c.4813G>A
MANE Select
|
ENSP00000498587.1:p.Val1605Ile
|
|
ENST00000679595.1:c.4813G>A
|
ENSP00000506241.1:p.Val1605Ile
|
|
ENST00000680133.1:c.4699G>A
|
ENSP00000505319.1:p.Val1567Ile
|
|
ENST00000680218.1:c.4693G>A
|
ENSP00000505339.1:p.Val1565Ile
|
|
ENST00000680668.1:c.4699G>A
|
ENSP00000506336.1:p.Val1567Ile
|
|
ENST00000680778.1:c.2410G>A
|
ENSP00000506033.1:p.Val804Ile
|
|
ENST00000680924.1:c.*2213G>A
|
ENSP00000506031.1:n.*2213G>A
|
|
ENST00000681135.1:c.*2422G>A
|
ENSP00000506636.1:n.*2422G>A
|
|
ENST00000681298.1:n.1626G>A
|
|
|
ENST00000681454.1:c.*4049G>A
|
ENSP00000505763.1:n.*4049G>A
|
|
ENST00000277541.6:c.4813G>A
|
ENSP00000277541.6:p.Val1605Ile
|
|
NM_017617.3:c.4813G>A
|
NP_060087.3:p.Val1605Ile
|
|
XM_011518717.1:c.4114G>A
|
XP_011517019.1:p.Val1372Ile
|
|
NM_017617.5:c.4813G>A
MANE Select
|
NP_060087.3:p.Val1605Ile
|
|
XM_011518717.2:c.4090G>A
|
XP_011517019.2:p.Val1364Ile
|
|