ENST00000578493.2:n.786T>G
|
|
|
ENST00000699291.1:c.578T>G
|
ENSP00000514272.1:n.578T>G
|
|
ENST00000699292.1:n.493T>G
|
|
|
ENST00000225275.4:c.1453T>G
MANE Select
|
ENSP00000225275.3:p.Ser485Ala
|
|
ENST00000225275.3:c.1453T>G
|
ENSP00000225275.3:p.Ser485Ala
|
|
NM_000250.1:c.1453T>G , LRG_84t1:c.1453T>G
|
NP_000241.1:p.Ser485Ala
|
|
XM_011524821.1:c.1639T>G
|
XP_011523123.1:p.Ser547Ala
|
|
XM_011524822.1:c.1168T>G
|
XP_011523124.1:p.Ser390Ala
|
|
XM_011524823.1:c.*2T>G
|
XP_011523125.1:n.*2T>G
|
|
NM_000250.2:c.1453T>G
MANE Select
|
NP_000241.1:p.Ser485Ala
|
|