ENST00000645828.1:n.2566A>T
|
|
|
ENST00000651671.1:c.4759A>T
MANE Select
|
ENSP00000498587.1:p.Asn1587Tyr
|
|
ENST00000679595.1:c.4759A>T
|
ENSP00000506241.1:p.Asn1587Tyr
|
|
ENST00000680133.1:c.4645A>T
|
ENSP00000505319.1:p.Asn1549Tyr
|
|
ENST00000680218.1:c.4639A>T
|
ENSP00000505339.1:p.Asn1547Tyr
|
|
ENST00000680668.1:c.4645A>T
|
ENSP00000506336.1:p.Asn1549Tyr
|
|
ENST00000680778.1:c.2356A>T
|
ENSP00000506033.1:p.Asn786Tyr
|
|
ENST00000680924.1:c.*2159A>T
|
ENSP00000506031.1:n.*2159A>T
|
|
ENST00000681135.1:c.*2368A>T
|
ENSP00000506636.1:n.*2368A>T
|
|
ENST00000681298.1:n.1572A>T
|
|
|
ENST00000681454.1:c.*3995A>T
|
ENSP00000505763.1:n.*3995A>T
|
|
ENST00000277541.6:c.4759A>T
|
ENSP00000277541.6:p.Asn1587Tyr
|
|
NM_017617.3:c.4759A>T
|
NP_060087.3:p.Asn1587Tyr
|
|
XM_011518717.1:c.4060A>T
|
XP_011517019.1:p.Asn1354Tyr
|
|
NM_017617.5:c.4759A>T
MANE Select
|
NP_060087.3:p.Asn1587Tyr
|
|
XM_011518717.2:c.4036A>T
|
XP_011517019.2:p.Asn1346Tyr
|
|