ENST00000578493.2:n.717T>A
|
|
|
ENST00000699291.1:c.509T>A
|
ENSP00000514272.1:p.Leu170Gln
|
|
ENST00000699292.1:n.424T>A
|
|
|
ENST00000225275.4:c.1384T>A
MANE Select
|
ENSP00000225275.3:p.Tyr462Asn
|
|
ENST00000225275.3:c.1384T>A
|
ENSP00000225275.3:p.Tyr462Asn
|
|
NM_000250.1:c.1384T>A , LRG_84t1:c.1384T>A
|
NP_000241.1:p.Tyr462Asn
|
|
XM_011524821.1:c.1570T>A
|
XP_011523123.1:p.Tyr524Asn
|
|
XM_011524822.1:c.1099T>A
|
XP_011523124.1:p.Tyr367Asn
|
|
XM_011524823.1:c.1409T>A
|
XP_011523125.1:p.Leu470Gln
|
|
NM_000250.2:c.1384T>A
MANE Select
|
NP_000241.1:p.Tyr462Asn
|
|