ENST00000578493.2:n.787C>G
|
|
|
ENST00000699291.1:c.579C>G
|
ENSP00000514272.1:n.579C>G
|
|
ENST00000699292.1:n.494C>G
|
|
|
ENST00000225275.4:c.1454C>G
MANE Select
|
ENSP00000225275.3:p.Ser485Ter
|
|
ENST00000225275.3:c.1454C>G
|
ENSP00000225275.3:p.Ser485Ter
|
|
NM_000250.1:c.1454C>G , LRG_84t1:c.1454C>G
|
NP_000241.1:p.Ser485Ter
|
|
XM_011524821.1:c.1640C>G
|
XP_011523123.1:p.Ser547Ter
|
|
XM_011524822.1:c.1169C>G
|
XP_011523124.1:p.Ser390Ter
|
|
XM_011524823.1:c.*3C>G
|
XP_011523125.1:n.*3C>G
|
|
NM_000250.2:c.1454C>G
MANE Select
|
NP_000241.1:p.Ser485Ter
|
|