ENST00000225927.7:c.1450G>C
MANE Select
|
ENSP00000225927.1:p.Gly484Arg
|
|
ENST00000225927.6:c.1450G>C
|
ENSP00000225927.1:p.Gly484Arg
|
|
ENST00000591587.1:c.788G>C
|
ENSP00000467836.1:n.788G>C
|
|
ENST00000592454.1:c.489G>C
|
|
|
NM_000263.3:c.1450G>C
|
NP_000254.2:p.Gly484Arg
|
|
XM_006721920.2:c.619G>C
|
XP_006721983.1:p.Gly207Arg
|
|
XM_011524840.1:c.451G>C
|
XP_011523142.1:p.Gly151Arg
|
|
XM_017024687.1:c.619G>C
|
XP_016880176.1:p.Gly207Arg
|
|
XM_024450771.1:c.1507G>C
|
XP_024306539.1:p.Gly503Arg
|
|
XM_024450772.1:c.451G>C
|
XP_024306540.1:p.Gly151Arg
|
|
NM_000263.4:c.1450G>C
MANE Select
|
NP_000254.2:p.Gly484Arg
|
|