ENST00000318471.5:c.893G>A
MANE Select
|
ENSP00000315680.3:p.Ser298Asn
|
|
ENST00000541292.6:c.*158G>A
|
ENSP00000441004.1:n.*158G>A
|
|
ENST00000678002.1:c.581G>A
|
|
|
ENST00000678557.1:c.779G>A
|
ENSP00000502962.1:p.Ser260Asn
|
|
ENST00000679286.1:c.773G>A
|
ENSP00000503168.1:p.Ser258Asn
|
|
ENST00000318471.4:c.893G>A
|
ENSP00000315680.3:p.Ser298Asn
|
|
NM_000288.3:c.893G>A
|
NP_000279.1:p.Ser298Asn
|
|
XM_005267019.3:c.779G>A
|
XP_005267076.1:p.Ser260Asn
|
|
XM_006715502.1:c.599G>A
|
XP_006715565.1:p.Ser200Asn
|
|
XM_005267019.4:c.779G>A
|
XP_005267076.1:p.Ser260Asn
|
|
XM_006715502.2:c.599G>A
|
XP_006715565.1:p.Ser200Asn
|
|
XM_017010934.2:c.*16G>A
|
XP_016866423.1:n.*16G>A
|
|
NM_000288.4:c.893G>A
MANE Select
|
NP_000279.1:p.Ser298Asn
|
|