ENST00000261208.8:c.800T>A
MANE Select
|
ENSP00000261208.3:p.Leu267Gln
|
|
ENST00000261208.7:c.800T>A
|
ENSP00000261208.3:p.Leu267Gln
|
|
ENST00000538703.5:c.800T>A
|
ENSP00000440861.1:p.Leu267Gln
|
|
ENST00000541929.5:c.176T>A
|
ENSP00000446364.1:p.Leu59Gln
|
|
ENST00000544080.6:c.*229T>A
|
ENSP00000439385.2:n.*229T>A
|
|
ENST00000546999.5:c.*229T>A
|
ENSP00000447675.1:n.*229T>A
|
|
ENST00000549376.1:n.193T>A
|
|
|
ENST00000551562.1:n.60T>A
|
|
|
ENST00000552509.5:c.764T>A
|
ENSP00000450372.1:p.Leu255Gln
|
|
NM_001258333.1:c.176T>A
|
NP_001245262.1:p.Leu59Gln
|
|
NM_001258334.1:c.800T>A
|
NP_001245263.1:p.Leu267Gln
|
|
NM_002108.3:c.800T>A
|
NP_002099.1:p.Leu267Gln
|
|
XM_011538249.1:c.4-2208T>A
|
XP_011536551.1:n.4-2208T>A
|
|
XM_011538249.2:c.4-2208T>A
|
XP_011536551.1:n.4-2208T>A
|
|
NM_002108.4:c.800T>A
MANE Select
|
NP_002099.1:p.Leu267Gln
|
|
NM_001258334.2:c.800T>A
|
NP_001245263.1:p.Leu267Gln
|
|
NM_001258333.2:c.176T>A
|
NP_001245262.1:p.Leu59Gln
|
|