ENST00000255078.8:c.2253T>G
MANE Select
|
ENSP00000255078.4:p.Asn751Lys
|
|
ENST00000674675.1:c.497T>G
|
|
|
ENST00000674878.1:c.497T>G
|
|
|
ENST00000674955.1:c.*970T>G
|
ENSP00000502463.1:n.*970T>G
|
|
ENST00000675118.1:c.1741T>G
|
|
|
ENST00000675389.1:n.528T>G
|
|
|
ENST00000675615.1:c.2253T>G
|
ENSP00000502413.1:p.Asn751Lys
|
|
ENST00000675648.1:n.1628T>G
|
|
|
ENST00000675916.1:c.497T>G
|
|
|
ENST00000676173.1:n.2998T>G
|
|
|
ENST00000676182.1:c.684T>G
|
|
|
ENST00000676228.1:c.*1576T>G
|
ENSP00000502375.1:n.*1576T>G
|
|
ENST00000255078.7:c.2253T>G
|
ENSP00000255078.3:p.Asn751Lys
|
|
ENST00000539064.5:n.2012T>G
|
|
|
ENST00000543739.5:n.1246T>G
|
|
|
NM_002180.2:c.2253T>G , LRG_250t1:c.2253T>G
|
NP_002171.2:p.Asn751Lys
|
|
XM_005273974.2:c.1242T>G
|
XP_005274031.1:p.Asn414Lys
|
|
XM_005273975.2:c.1125T>G
|
XP_005274032.1:p.Asn375Lys
|
|
XM_011544994.1:c.1020T>G
|
XP_011543296.1:p.Asn340Lys
|
|
XR_949903.1:n.2355T>G
|
|
|
XM_005273975.3:c.1125T>G
|
XP_005274032.1:p.Asn375Lys
|
|
XM_017017669.2:c.1242T>G
|
XP_016873158.1:p.Asn414Lys
|
|
XM_017017670.2:c.1242T>G
|
XP_016873159.1:p.Asn414Lys
|
|
XR_949903.3:n.2351T>G
|
|
|
NM_002180.3:c.2253T>G
MANE Select
|
NP_002171.2:p.Asn751Lys
|
|