ENST00000261208.8:c.816G>T
MANE Select
|
ENSP00000261208.3:p.Lys272Asn
|
|
ENST00000261208.7:c.816G>T
|
ENSP00000261208.3:p.Lys272Asn
|
|
ENST00000538703.5:c.816G>T
|
ENSP00000440861.1:p.Lys272Asn
|
|
ENST00000541929.5:c.192G>T
|
ENSP00000446364.1:p.Lys64Asn
|
|
ENST00000544080.6:c.*245G>T
|
ENSP00000439385.2:n.*245G>T
|
|
ENST00000546999.5:c.*245G>T
|
ENSP00000447675.1:n.*245G>T
|
|
ENST00000549376.1:n.209G>T
|
|
|
ENST00000551562.1:n.76G>T
|
|
|
ENST00000552509.5:c.780G>T
|
ENSP00000450372.1:p.Lys260Asn
|
|
NM_001258333.1:c.192G>T
|
NP_001245262.1:p.Lys64Asn
|
|
NM_001258334.1:c.816G>T
|
NP_001245263.1:p.Lys272Asn
|
|
NM_002108.3:c.816G>T
|
NP_002099.1:p.Lys272Asn
|
|
XM_011538249.1:c.4-2192G>T
|
XP_011536551.1:n.4-2192G>T
|
|
XM_011538249.2:c.4-2192G>T
|
XP_011536551.1:n.4-2192G>T
|
|
NM_002108.4:c.816G>T
MANE Select
|
NP_002099.1:p.Lys272Asn
|
|
NM_001258334.2:c.816G>T
|
NP_001245263.1:p.Lys272Asn
|
|
NM_001258333.2:c.192G>T
|
NP_001245262.1:p.Lys64Asn
|
|