ENST00000231749.8:c.586G>A
MANE Select
|
ENSP00000231749.3:p.Asp196Asn
|
|
ENST00000231749.7:c.586G>A
|
ENSP00000231749.3:p.Asp196Asn
|
|
ENST00000360165.7:c.586G>A
|
ENSP00000353289.3:p.Asp196Asn
|
|
ENST00000442887.1:c.457G>A
|
ENSP00000393687.1:p.Asp153Asn
|
|
ENST00000443080.5:c.*338G>A
|
ENSP00000415661.1:n.*338G>A
|
|
ENST00000475688.1:n.38G>A
|
|
|
NM_001308379.1:c.586G>A
|
NP_001295308.1:p.Asp196Asn
|
|
NM_015896.2:c.586G>A
|
NP_056980.2:p.Asp196Asn
|
|
NM_015896.3:c.586G>A
|
NP_056980.2:p.Asp196Asn
|
|
XM_005265216.2:c.349G>A
|
XP_005265273.1:p.Asp117Asn
|
|
XM_005265216.3:c.349G>A
|
XP_005265273.1:p.Asp117Asn
|
|
NM_015896.4:c.586G>A
MANE Select
|
NP_056980.2:p.Asp196Asn
|
|
NM_001308379.2:c.586G>A
|
NP_001295308.1:p.Asp196Asn
|
|