ENST00000367408.6:n.2957A>G
|
|
|
ENST00000367409.9:c.9670A>G
MANE Select
|
ENSP00000356379.4:p.Asn3224Asp
|
|
ENST00000680265.1:c.9892A>G
|
ENSP00000505384.1:p.Asn3298Asp
|
|
ENST00000680710.1:c.9646A>G
|
ENSP00000506676.1:p.Asn3216Asp
|
|
ENST00000294732.11:c.4915A>G
|
ENSP00000294732.7:p.Asn1639Asp
|
|
ENST00000367408.5:c.2665A>G
|
ENSP00000356378.1:p.Asn889Asp
|
|
ENST00000367409.8:c.9670A>G
|
ENSP00000356379.4:p.Asn3224Asp
|
|
ENST00000612785.1:c.3628A>G
|
ENSP00000479244.1:p.Asn1210Asp
|
|
NM_001206846.1:c.4915A>G
|
NP_001193775.1:p.Asn1639Asp
|
|
NM_018136.4:c.9670A>G
|
NP_060606.3:p.Asn3224Asp
|
|
NM_018136.5:c.9670A>G
MANE Select
|
NP_060606.3:p.Asn3224Asp
|
|
NM_001206846.2:c.4915A>G
|
NP_001193775.1:p.Asn1639Asp
|
|