ENST00000645828.1:n.2567A>C
|
|
|
ENST00000651671.1:c.4760A>C
MANE Select
|
ENSP00000498587.1:p.Asn1587Thr
|
|
ENST00000679595.1:c.4760A>C
|
ENSP00000506241.1:p.Asn1587Thr
|
|
ENST00000680133.1:c.4646A>C
|
ENSP00000505319.1:p.Asn1549Thr
|
|
ENST00000680218.1:c.4640A>C
|
ENSP00000505339.1:p.Asn1547Thr
|
|
ENST00000680668.1:c.4646A>C
|
ENSP00000506336.1:p.Asn1549Thr
|
|
ENST00000680778.1:c.2357A>C
|
ENSP00000506033.1:p.Asn786Thr
|
|
ENST00000680924.1:c.*2160A>C
|
ENSP00000506031.1:n.*2160A>C
|
|
ENST00000681135.1:c.*2369A>C
|
ENSP00000506636.1:n.*2369A>C
|
|
ENST00000681298.1:n.1573A>C
|
|
|
ENST00000681454.1:c.*3996A>C
|
ENSP00000505763.1:n.*3996A>C
|
|
ENST00000277541.6:c.4760A>C
|
ENSP00000277541.6:p.Asn1587Thr
|
|
NM_017617.3:c.4760A>C
|
NP_060087.3:p.Asn1587Thr
|
|
XM_011518717.1:c.4061A>C
|
XP_011517019.1:p.Asn1354Thr
|
|
NM_017617.5:c.4760A>C
MANE Select
|
NP_060087.3:p.Asn1587Thr
|
|
XM_011518717.2:c.4037A>C
|
XP_011517019.2:p.Asn1346Thr
|
|