ENST00000682422.1:n.837T>A
|
|
|
ENST00000682545.1:c.*262T>A
|
ENSP00000508402.1:n.*262T>A
|
|
ENST00000682887.1:c.1657T>A
|
ENSP00000506946.1:n.1657T>A
|
|
ENST00000683302.1:c.1187T>A
|
ENSP00000507885.1:p.Ile396Asn
|
|
ENST00000683557.1:c.*88T>A
|
ENSP00000508029.1:n.*88T>A
|
|
ENST00000367282.6:c.1256T>A
MANE Select
|
ENSP00000356251.4:p.Ile419Asn
|
|
ENST00000367282.5:c.1256T>A
|
ENSP00000356251.4:p.Ile419Asn
|
|
NM_004767.3:c.1256T>A
|
NP_004758.3:p.Ile419Asn
|
|
XM_011510158.1:c.695T>A
|
XP_011508460.1:p.Ile232Asn
|
|
NM_004767.4:c.1256T>A
|
NP_004758.3:p.Ile419Asn
|
|
XM_011510158.2:c.695T>A
|
XP_011508460.1:p.Ile232Asn
|
|
NM_004767.5:c.1256T>A
MANE Select
|
NP_004758.3:p.Ile419Asn
|
|