ENST00000578493.2:n.909C>A
|
|
|
ENST00000699291.1:c.701C>A
|
ENSP00000514272.1:n.701C>A
|
|
ENST00000699292.1:n.616C>A
|
|
|
ENST00000225275.4:c.1576C>A
MANE Select
|
ENSP00000225275.3:p.Pro526Thr
|
|
ENST00000225275.3:c.1576C>A
|
ENSP00000225275.3:p.Pro526Thr
|
|
ENST00000577220.1:c.34C>A
|
ENSP00000464668.1:p.Pro12Thr
|
|
NM_000250.1:c.1576C>A , LRG_84t1:c.1576C>A
|
NP_000241.1:p.Pro526Thr
|
|
XM_011524821.1:c.1762C>A
|
XP_011523123.1:p.Pro588Thr
|
|
XM_011524822.1:c.1291C>A
|
XP_011523124.1:p.Pro431Thr
|
|
XM_011524823.1:c.*125C>A
|
XP_011523125.1:n.*125C>A
|
|
NM_000250.2:c.1576C>A
MANE Select
|
NP_000241.1:p.Pro526Thr
|
|