ENST00000225927.7:c.1387T>A
MANE Select
|
ENSP00000225927.1:p.Trp463Arg
|
|
ENST00000225927.6:c.1387T>A
|
ENSP00000225927.1:p.Trp463Arg
|
|
ENST00000591587.1:c.725T>A
|
ENSP00000467836.1:n.725T>A
|
|
ENST00000592454.1:c.426T>A
|
|
|
NM_000263.3:c.1387T>A
|
NP_000254.2:p.Trp463Arg
|
|
XM_006721920.2:c.556T>A
|
XP_006721983.1:p.Trp186Arg
|
|
XM_011524840.1:c.388T>A
|
XP_011523142.1:p.Trp130Arg
|
|
XM_017024687.1:c.556T>A
|
XP_016880176.1:p.Trp186Arg
|
|
XM_024450771.1:c.1444T>A
|
XP_024306539.1:p.Trp482Arg
|
|
XM_024450772.1:c.388T>A
|
XP_024306540.1:p.Trp130Arg
|
|
NM_000263.4:c.1387T>A
MANE Select
|
NP_000254.2:p.Trp463Arg
|
|