ENST00000225927.7:c.1614G>T
MANE Select
|
ENSP00000225927.1:p.Glu538Asp
|
|
ENST00000225927.6:c.1614G>T
|
ENSP00000225927.1:p.Glu538Asp
|
|
ENST00000591587.1:c.952G>T
|
ENSP00000467836.1:n.952G>T
|
|
NM_000263.3:c.1614G>T
|
NP_000254.2:p.Glu538Asp
|
|
XM_006721920.2:c.783G>T
|
XP_006721983.1:p.Glu261Asp
|
|
XM_011524840.1:c.615G>T
|
XP_011523142.1:p.Glu205Asp
|
|
XM_017024687.1:c.783G>T
|
XP_016880176.1:p.Glu261Asp
|
|
XM_024450771.1:c.1671G>T
|
XP_024306539.1:p.Glu557Asp
|
|
XM_024450772.1:c.615G>T
|
XP_024306540.1:p.Glu205Asp
|
|
NM_000263.4:c.1614G>T
MANE Select
|
NP_000254.2:p.Glu538Asp
|
|