ENST00000647165.2:c.7123G>A
MANE Select
|
ENSP00000495481.1:p.Asp2375Asn
|
|
ENST00000205890.9:c.7123G>A
|
ENSP00000205890.5:p.Asp2375Asn
|
|
ENST00000578999.1:n.744G>A
|
|
|
ENST00000615845.4:c.7123G>A
|
ENSP00000481642.1:p.Asp2375Asn
|
|
NM_016239.3:c.7123G>A
|
NP_057323.3:p.Asp2375Asn
|
|
XM_011523917.1:c.6798G>A
|
XP_011522219.1:p.Gln2266=
|
|
XM_011523921.1:c.7117G>A
|
XP_011522223.1:p.Asp2373Asn
|
|
XR_934037.1:n.7457G>A
|
|
|
XR_934038.1:n.7409G>A
|
|
|
XR_934293.1:n.435-1885C>T
|
|
|
XR_934295.1:n.254-1885C>T
|
|
|
XM_017024714.2:c.7063G>A
|
XP_016880203.1:p.Asp2355Asn
|
|
XM_017024715.2:c.7126G>A
|
XP_016880204.1:p.Asp2376Asn
|
|
XR_934293.2:n.378-1885C>T
|
|
|
NM_016239.4:c.7123G>A
MANE Select
|
NP_057323.3:p.Asp2375Asn
|
|