ENST00000578493.2:n.703T>G
|
|
|
ENST00000699291.1:c.495T>G
|
ENSP00000514272.1:p.His165Gln
|
|
ENST00000699292.1:n.410T>G
|
|
|
ENST00000225275.4:c.1370T>G
MANE Select
|
ENSP00000225275.3:p.Ile457Ser
|
|
ENST00000225275.3:c.1370T>G
|
ENSP00000225275.3:p.Ile457Ser
|
|
NM_000250.1:c.1370T>G , LRG_84t1:c.1370T>G
|
NP_000241.1:p.Ile457Ser
|
|
XM_011524821.1:c.1556T>G
|
XP_011523123.1:p.Ile519Ser
|
|
XM_011524822.1:c.1085T>G
|
XP_011523124.1:p.Ile362Ser
|
|
XM_011524823.1:c.1395T>G
|
XP_011523125.1:p.His465Gln
|
|
NM_000250.2:c.1370T>G
MANE Select
|
NP_000241.1:p.Ile457Ser
|
|