ENST00000249750.9:c.470T>A
MANE Select
|
ENSP00000249750.4:p.Ile157Asn
|
|
ENST00000249750.8:c.470T>A
|
ENSP00000249750.4:p.Ile157Asn
|
|
ENST00000347587.7:c.470T>A
|
ENSP00000309623.3:p.Ile157Asn
|
|
ENST00000430119.6:c.*444T>A
|
ENSP00000416754.2:n.*444T>A
|
|
ENST00000537372.5:c.407T>A
|
ENSP00000438296.1:p.Ile136Asn
|
|
ENST00000558231.5:c.383T>A
|
ENSP00000453600.1:p.Ile128Asn
|
|
ENST00000559266.5:n.318+3186T>A
|
|
|
ENST00000559517.5:c.182T>A
|
ENSP00000453408.1:p.Ile61Asn
|
|
ENST00000561070.5:c.182T>A
|
ENSP00000452850.1:p.Ile61Asn
|
|
NM_001206897.1:c.407T>A
|
NP_001193826.1:p.Ile136Asn
|
|
NM_003888.3:c.470T>A
|
NP_003879.2:p.Ile157Asn
|
|
NM_170696.2:c.470T>A
|
NP_733797.1:p.Ile157Asn
|
|
NM_170697.2:c.182T>A
|
NP_733798.1:p.Ile61Asn
|
|
XM_024450095.1:c.470T>A
|
XP_024305863.1:p.Ile157Asn
|
|
NM_003888.4:c.470T>A
MANE Select
|
NP_003879.2:p.Ile157Asn
|
|
NM_170696.3:c.470T>A
|
NP_733797.1:p.Ile157Asn
|
|
NM_170697.3:c.182T>A
|
NP_733798.1:p.Ile61Asn
|
|
NM_001206897.2:c.407T>A
|
NP_001193826.1:p.Ile136Asn
|
|