ENST00000225927.7:c.2114A>T
MANE Select
|
ENSP00000225927.1:p.Glu705Val
|
|
ENST00000225927.6:c.2114A>T
|
ENSP00000225927.1:p.Glu705Val
|
|
ENST00000591587.1:c.1452A>T
|
ENSP00000467836.1:n.1452A>T
|
|
NM_000263.3:c.2114A>T
|
NP_000254.2:p.Glu705Val
|
|
XM_006721920.2:c.1283A>T
|
XP_006721983.1:p.Glu428Val
|
|
XM_011524840.1:c.1115A>T
|
XP_011523142.1:p.Glu372Val
|
|
XM_017024687.1:c.1283A>T
|
XP_016880176.1:p.Glu428Val
|
|
XM_024450771.1:c.2171A>T
|
XP_024306539.1:p.Glu724Val
|
|
XM_024450772.1:c.1115A>T
|
XP_024306540.1:p.Glu372Val
|
|
NM_000263.4:c.2114A>T
MANE Select
|
NP_000254.2:p.Glu705Val
|
|