ENST00000249750.9:c.486T>C
MANE Select
|
ENSP00000249750.4:p.Ile162=
|
|
ENST00000249750.8:c.486T>C
|
ENSP00000249750.4:p.Ile162=
|
|
ENST00000347587.7:c.486T>C
|
ENSP00000309623.3:p.Ile162=
|
|
ENST00000430119.6:c.*460T>C
|
ENSP00000416754.2:n.*460T>C
|
|
ENST00000537372.5:c.423T>C
|
ENSP00000438296.1:p.Ile141=
|
|
ENST00000558231.5:c.399T>C
|
ENSP00000453600.1:p.Ile133=
|
|
ENST00000559266.5:n.318+3202T>C
|
|
|
ENST00000559517.5:c.198T>C
|
ENSP00000453408.1:p.Ile66=
|
|
ENST00000561070.5:c.198T>C
|
ENSP00000452850.1:p.Ile66=
|
|
NM_001206897.1:c.423T>C
|
NP_001193826.1:p.Ile141=
|
|
NM_003888.3:c.486T>C
|
NP_003879.2:p.Ile162=
|
|
NM_170696.2:c.486T>C
|
NP_733797.1:p.Ile162=
|
|
NM_170697.2:c.198T>C
|
NP_733798.1:p.Ile66=
|
|
XM_024450095.1:c.486T>C
|
XP_024305863.1:p.Ile162=
|
|
NM_003888.4:c.486T>C
MANE Select
|
NP_003879.2:p.Ile162=
|
|
NM_170696.3:c.486T>C
|
NP_733797.1:p.Ile162=
|
|
NM_170697.3:c.198T>C
|
NP_733798.1:p.Ile66=
|
|
NM_001206897.2:c.423T>C
|
NP_001193826.1:p.Ile141=
|
|