ENST00000682565.1:c.10030A>C
|
ENSP00000507671.1:p.Asn3344His
|
|
ENST00000682801.1:c.10030A>C
|
ENSP00000507862.1:p.Asn3344His
|
|
ENST00000682859.1:c.10030A>C
|
ENSP00000508222.1:p.Asn3344His
|
|
ENST00000683791.1:c.3116A>C
|
|
|
ENST00000684460.1:c.7311A>C
|
|
|
ENST00000684548.1:c.10030A>C
|
ENSP00000507421.1:p.Asn3344His
|
|
ENST00000684590.1:c.4477A>C
|
ENSP00000507376.1:p.Asn1493His
|
|
ENST00000684656.1:c.7356A>C
|
|
|
ENST00000613296.6:c.10411A>C
MANE Select
|
ENSP00000482968.1:p.Asn3471His
|
|
ENST00000651057.1:c.565A>C
|
ENSP00000498504.1:p.Asn189His
|
|
ENST00000651434.1:c.1767A>C
|
|
|
ENST00000652487.1:c.1508A>C
|
|
|
ENST00000423048.5:c.3902A>C
|
ENSP00000399833.1:n.3902A>C
|
|
ENST00000484298.5:c.10285A>C
|
ENSP00000478155.1:p.Asn3429His
|
|
ENST00000613296.4:c.10411A>C
|
ENSP00000482968.1:p.Asn3471His
|
|
ENST00000614410.4:c.10411A>C
|
ENSP00000479094.1:p.Asn3471His
|
|
ENST00000620466.4:n.4214A>C
|
|
|
NM_015120.4:c.10414A>C , LRG_741t1:c.10414A>C
|
NP_055935.4:p.Asn3472His
|
|
NM_001378454.1:c.10411A>C
MANE Select
|
NP_001365383.1:p.Asn3471His
|
|