ENST00000261208.8:c.801A>G
MANE Select
|
ENSP00000261208.3:p.Leu267=
|
|
ENST00000261208.7:c.801A>G
|
ENSP00000261208.3:p.Leu267=
|
|
ENST00000538703.5:c.801A>G
|
ENSP00000440861.1:p.Leu267=
|
|
ENST00000541929.5:c.177A>G
|
ENSP00000446364.1:p.Leu59=
|
|
ENST00000544080.6:c.*230A>G
|
ENSP00000439385.2:n.*230A>G
|
|
ENST00000546999.5:c.*230A>G
|
ENSP00000447675.1:n.*230A>G
|
|
ENST00000549376.1:n.194A>G
|
|
|
ENST00000551562.1:n.61A>G
|
|
|
ENST00000552509.5:c.765A>G
|
ENSP00000450372.1:p.Leu255=
|
|
NM_001258333.1:c.177A>G
|
NP_001245262.1:p.Leu59=
|
|
NM_001258334.1:c.801A>G
|
NP_001245263.1:p.Leu267=
|
|
NM_002108.3:c.801A>G
|
NP_002099.1:p.Leu267=
|
|
XM_011538249.1:c.4-2207A>G
|
XP_011536551.1:n.4-2207A>G
|
|
XM_011538249.2:c.4-2207A>G
|
XP_011536551.1:n.4-2207A>G
|
|
NM_002108.4:c.801A>G
MANE Select
|
NP_002099.1:p.Leu267=
|
|
NM_001258334.2:c.801A>G
|
NP_001245263.1:p.Leu267=
|
|
NM_001258333.2:c.177A>G
|
NP_001245262.1:p.Leu59=
|
|