ENST00000651671.1:c.6348C>A
MANE Select
|
ENSP00000498587.1:p.Tyr2116Ter
|
|
ENST00000679595.1:c.*1388C>A
|
ENSP00000506241.1:n.*1388C>A
|
|
ENST00000679969.1:n.2944C>A
|
|
|
ENST00000680003.1:n.2680C>A
|
|
|
ENST00000680133.1:c.6234C>A
|
ENSP00000505319.1:p.Tyr2078Ter
|
|
ENST00000680218.1:c.6228C>A
|
ENSP00000505339.1:p.Tyr2076Ter
|
|
ENST00000680668.1:c.6234C>A
|
ENSP00000506336.1:p.Tyr2078Ter
|
|
ENST00000680778.1:c.3945C>A
|
ENSP00000506033.1:p.Tyr1315Ter
|
|
ENST00000680924.1:c.*3748C>A
|
ENSP00000506031.1:n.*3748C>A
|
|
ENST00000681135.1:c.*3957C>A
|
ENSP00000506636.1:n.*3957C>A
|
|
ENST00000681298.1:n.4453C>A
|
|
|
ENST00000681454.1:c.*5584C>A
|
ENSP00000505763.1:n.*5584C>A
|
|
ENST00000277541.6:c.6348C>A
|
ENSP00000277541.6:p.Tyr2116Ter
|
|
NM_017617.3:c.6348C>A
|
NP_060087.3:p.Tyr2116Ter
|
|
XM_011518717.1:c.5649C>A
|
XP_011517019.1:p.Tyr1883Ter
|
|
NM_017617.5:c.6348C>A
MANE Select
|
NP_060087.3:p.Tyr2116Ter
|
|
XM_011518717.2:c.5625C>A
|
XP_011517019.2:p.Tyr1875Ter
|
|