ENST00000555238.6:c.1780G>A
MANE Select
|
ENSP00000451300.1:p.Asp594Asn
|
|
ENST00000355058.7:c.1780G>A
|
ENSP00000347169.3:p.Asp594Asn
|
|
ENST00000356296.8:c.1636G>A
|
ENSP00000348644.4:p.Asp546Asn
|
|
ENST00000359560.7:c.1747G>A
|
ENSP00000352563.3:p.Asp583Asn
|
|
ENST00000535282.5:c.1636G>A
|
ENSP00000441258.2:p.Asp546Asn
|
|
ENST00000544991.7:c.1195G>A
|
ENSP00000446001.3:p.Asp399Asn
|
|
ENST00000554521.6:c.1162G>A
|
ENSP00000450817.2:p.Asp388Asn
|
|
ENST00000554546.5:c.1603G>A
|
ENSP00000452416.1:p.Asp535Asn
|
|
ENST00000555238.5:c.1780G>A
|
ENSP00000451300.1:p.Asp594Asn
|
|
ENST00000555394.5:c.1636G>A
|
ENSP00000451625.1:p.Asp546Asn
|
|
ENST00000555738.6:c.1309G>A
|
ENSP00000452069.2:p.Asp437Asn
|
|
ENST00000556772.5:c.1348G>A
|
ENSP00000451513.1:p.Asp450Asn
|
|
ENST00000557597.5:c.1747G>A
|
ENSP00000451117.1:p.Asp583Asn
|
|
ENST00000559312.5:c.1195G>A
|
ENSP00000452888.1:p.Asp399Asn
|
|
ENST00000560335.5:c.1342G>A
|
ENSP00000453209.1:p.Asp448Asn
|
|
NM_001005743.1:c.1780G>A
|
NP_001005743.1:p.Asp594Asn
|
|
NM_001005744.1:c.1636G>A
|
NP_001005744.1:p.Asp546Asn
|
|
NM_001005745.1:c.1603G>A
|
NP_001005745.1:p.Asp535Asn
|
|
NM_003744.5:c.1747G>A
|
NP_003735.3:p.Asp583Asn
|
|
XM_005268142.3:c.1780G>A
|
XP_005268199.1:p.Asp594Asn
|
|
XM_005268144.3:c.1747G>A
|
XP_005268201.1:p.Asp583Asn
|
|
XM_005268145.3:c.1738G>A
|
XP_005268202.1:p.Asp580Asn
|
|
XM_005268146.3:c.1636G>A
|
XP_005268203.1:p.Asp546Asn
|
|
XM_011537253.1:c.1780G>A
|
XP_011535555.1:p.Asp594Asn
|
|
XM_011537254.1:c.1780G>A
|
XP_011535556.1:p.Asp594Asn
|
|
XM_011537255.1:c.1780G>A
|
XP_011535557.1:p.Asp594Asn
|
|
XM_011537256.1:c.1771G>A
|
XP_011535558.1:p.Asp591Asn
|
|
XM_011537257.1:c.1747G>A
|
XP_011535559.1:p.Asp583Asn
|
|
XM_011537258.1:c.1747G>A
|
XP_011535560.1:p.Asp583Asn
|
|
XM_011537259.1:c.1738G>A
|
XP_011535561.1:p.Asp580Asn
|
|
XM_011537260.1:c.1636G>A
|
XP_011535562.1:p.Asp546Asn
|
|
XM_011537261.1:c.1627G>A
|
XP_011535563.1:p.Asp543Asn
|
|
XM_011537262.1:c.1486G>A
|
XP_011535564.1:p.Asp496Asn
|
|
XM_011537263.1:c.1342G>A
|
XP_011535565.1:p.Asp448Asn
|
|
XM_011537264.1:c.1309G>A
|
XP_011535566.1:p.Asp437Asn
|
|
NM_001320114.1:c.1636G>A
|
NP_001307043.1:p.Asp546Asn
|
|
NM_001005743.2:c.1780G>A
MANE Select
|
NP_001005743.1:p.Asp594Asn
|
|
NM_001005744.2:c.1636G>A
|
NP_001005744.1:p.Asp546Asn
|
|
NM_001005745.2:c.1603G>A
|
NP_001005745.1:p.Asp535Asn
|
|
NM_001320114.2:c.1636G>A
|
NP_001307043.1:p.Asp546Asn
|
|
NM_003744.6:c.1747G>A
|
NP_003735.3:p.Asp583Asn
|
|