ENST00000463045.3:c.268T>A
|
ENSP00000481376.2:p.Tyr90Asn
|
|
ENST00000491274.6:c.397T>A
|
ENSP00000480482.2:p.Tyr133Asn
|
|
ENST00000375499.8:c.439T>A
MANE Select
|
ENSP00000364649.3:p.Tyr147Asn
|
|
ENST00000375499.7:c.439T>A
|
ENSP00000364649.3:p.Tyr147Asn
|
|
ENST00000463045.2:c.268T>A
|
ENSP00000481376.1:p.Tyr90Asn
|
|
ENST00000475506.1:n.356T>A
|
|
|
ENST00000485515.5:n.373T>A
|
|
|
ENST00000491274.5:c.397T>A
|
ENSP00000480482.1:p.Tyr133Asn
|
|
NM_003000.2:c.439T>A , LRG_316t1:c.439T>A
|
NP_002991.2:p.Tyr147Asn
|
|
NM_003000.3:c.439T>A
MANE Select
|
NP_002991.2:p.Tyr147Asn
|
|