ENST00000249750.9:c.485T>G
MANE Select
|
ENSP00000249750.4:p.Ile162Ser
|
|
ENST00000249750.8:c.485T>G
|
ENSP00000249750.4:p.Ile162Ser
|
|
ENST00000347587.7:c.485T>G
|
ENSP00000309623.3:p.Ile162Ser
|
|
ENST00000430119.6:c.*459T>G
|
ENSP00000416754.2:n.*459T>G
|
|
ENST00000537372.5:c.422T>G
|
ENSP00000438296.1:p.Ile141Ser
|
|
ENST00000558231.5:c.398T>G
|
ENSP00000453600.1:p.Ile133Ser
|
|
ENST00000559266.5:n.318+3201T>G
|
|
|
ENST00000559517.5:c.197T>G
|
ENSP00000453408.1:p.Ile66Ser
|
|
ENST00000561070.5:c.197T>G
|
ENSP00000452850.1:p.Ile66Ser
|
|
NM_001206897.1:c.422T>G
|
NP_001193826.1:p.Ile141Ser
|
|
NM_003888.3:c.485T>G
|
NP_003879.2:p.Ile162Ser
|
|
NM_170696.2:c.485T>G
|
NP_733797.1:p.Ile162Ser
|
|
NM_170697.2:c.197T>G
|
NP_733798.1:p.Ile66Ser
|
|
XM_024450095.1:c.485T>G
|
XP_024305863.1:p.Ile162Ser
|
|
NM_003888.4:c.485T>G
MANE Select
|
NP_003879.2:p.Ile162Ser
|
|
NM_170696.3:c.485T>G
|
NP_733797.1:p.Ile162Ser
|
|
NM_170697.3:c.197T>G
|
NP_733798.1:p.Ile66Ser
|
|
NM_001206897.2:c.422T>G
|
NP_001193826.1:p.Ile141Ser
|
|