|
NM_017617.5:c.4847T>A
MANE Select
|
NP_060087.3:p.Ile1616Asn
|
|
ENST00000651671.1:c.4847T>A
MANE Select
|
ENSP00000498587.1:p.Ile1616Asn
|
|
NM_017617.3:c.4847T>A
|
NP_060087.3:p.Ile1616Asn
|
|
ENST00000277541.6:c.4847T>A
|
ENSP00000277541.6:p.Ile1616Asn
|
|
ENST00000494783.1:n.2T>A
|
|
|
ENST00000645828.1:n.2654T>A
|
|
|
ENST00000679595.1:c.4847T>A
|
ENSP00000506241.1:p.Ile1616Asn
|
|
ENST00000680133.1:c.4733T>A
|
ENSP00000505319.1:p.Ile1578Asn
|
|
ENST00000680218.1:c.4727T>A
|
ENSP00000505339.1:p.Ile1576Asn
|
|
ENST00000680668.1:c.4733T>A
|
ENSP00000506336.1:p.Ile1578Asn
|
|
ENST00000680778.1:c.2444T>A
|
ENSP00000506033.1:p.Ile815Asn
|
|
ENST00000680924.1:c.*2247T>A
|
ENSP00000506031.1:n.*2247T>A
|
|
ENST00000681135.1:c.*2456T>A
|
ENSP00000506636.1:n.*2456T>A
|
|
ENST00000681298.1:n.1660T>A
|
|
|
ENST00000681454.1:c.*4083T>A
|
ENSP00000505763.1:n.*4083T>A
|
|
XM_011518717.1:c.4148T>A
|
XP_011517019.1:p.Ile1383Asn
|
|
XM_011518717.2:c.4124T>A
|
XP_011517019.2:p.Ile1375Asn
|
