ENST00000578493.2:n.907T>G
|
|
|
ENST00000699291.1:c.699T>G
|
ENSP00000514272.1:n.699T>G
|
|
ENST00000699292.1:n.614T>G
|
|
|
ENST00000225275.4:c.1574T>G
MANE Select
|
ENSP00000225275.3:p.Val525Gly
|
|
ENST00000225275.3:c.1574T>G
|
ENSP00000225275.3:p.Val525Gly
|
|
ENST00000577220.1:c.32T>G
|
ENSP00000464668.1:p.Val11Gly
|
|
NM_000250.1:c.1574T>G , LRG_84t1:c.1574T>G
|
NP_000241.1:p.Val525Gly
|
|
XM_011524821.1:c.1760T>G
|
XP_011523123.1:p.Val587Gly
|
|
XM_011524822.1:c.1289T>G
|
XP_011523124.1:p.Val430Gly
|
|
XM_011524823.1:c.*123T>G
|
XP_011523125.1:n.*123T>G
|
|
NM_000250.2:c.1574T>G
MANE Select
|
NP_000241.1:p.Val525Gly
|
|