ENST00000225927.7:c.2127T>A
MANE Select
|
ENSP00000225927.1:p.Val709=
|
|
ENST00000225927.6:c.2127T>A
|
ENSP00000225927.1:p.Val709=
|
|
ENST00000591587.1:c.1465T>A
|
ENSP00000467836.1:n.1465T>A
|
|
NM_000263.3:c.2127T>A
|
NP_000254.2:p.Val709=
|
|
XM_006721920.2:c.1296T>A
|
XP_006721983.1:p.Val432=
|
|
XM_011524840.1:c.1128T>A
|
XP_011523142.1:p.Val376=
|
|
XM_017024687.1:c.1296T>A
|
XP_016880176.1:p.Val432=
|
|
XM_024450771.1:c.2184T>A
|
XP_024306539.1:p.Val728=
|
|
XM_024450772.1:c.1128T>A
|
XP_024306540.1:p.Val376=
|
|
NM_000263.4:c.2127T>A
MANE Select
|
NP_000254.2:p.Val709=
|
|