ENST00000400521.7:c.1172A=
MANE Select
|
ENSP00000383365.1:p.Asp391=
|
|
ENST00000400518.5:c.1082A=
|
ENSP00000383362.1:p.Asp361=
|
|
ENST00000400519.6:c.1169A=
|
ENSP00000383363.1:p.Asp390=
|
|
ENST00000400521.6:c.1172A=
|
ENSP00000383365.1:p.Asp391=
|
|
ENST00000400525.6:c.1103A=
|
ENSP00000383369.3:p.Asp368=
|
|
ENST00000462330.5:c.95A=
|
ENSP00000485603.2:p.Asp32=
|
|
ENST00000462843.2:c.122A=
|
ENSP00000485466.2:p.Asp41=
|
|
ENST00000474308.5:c.1115A=
|
ENSP00000485665.1:p.Asp372=
|
|
ENST00000485358.5:c.140A=
|
ENSP00000485499.2:p.Asp47=
|
|
ENST00000487165.5:n.1266A=
|
|
|
ENST00000494454.5:n.1246A=
|
|
|
ENST00000495655.2:n.716A=
|
|
|
ENST00000542719.6:c.884A=
|
ENSP00000485128.2:p.Asp295=
|
|
ENST00000634471.1:n.244-361A=
|
|
|
ENST00000634537.1:c.401A=
|
ENSP00000489208.1:p.Asp134=
|
|
NM_006440.4:c.1172A=
|
NP_006431.2:p.Asp391=
|
|
NM_001352300.1:c.1169A=
|
NP_001339229.1:p.Asp390=
|
|
NM_001352301.1:c.1082A=
|
NP_001339230.1:p.Asp361=
|
|
NM_001352302.1:c.884A=
|
NP_001339231.1:p.Asp295=
|
|
NR_147957.1:n.1304A=
|
|
|
NM_006440.5:c.1172A=
MANE Select
|
NP_006431.2:p.Asp391=
|
|
NM_001352300.2:c.1169A=
|
NP_001339229.1:p.Asp390=
|
|
NR_147957.2:n.1130A=
|
|
|
NM_001352301.2:c.1082A=
|
NP_001339230.1:p.Asp361=
|
|
NM_001352302.2:c.884A=
|
NP_001339231.1:p.Asp295=
|
|