ENST00000305883.6:c.897A>G
MANE Select
|
ENSP00000307023.1:p.Leu299=
|
|
ENST00000305883.5:c.897A>G
|
ENSP00000307023.1:p.Leu299=
|
|
ENST00000535335.1:c.846A>G
|
ENSP00000442722.1:p.Leu282=
|
|
ENST00000540845.5:c.846A>G
|
ENSP00000444690.1:p.Leu282=
|
|
NM_001177716.1:c.846A>G
|
NP_001171187.1:p.Leu282=
|
|
NM_001177718.1:c.846A>G
|
NP_001171189.1:p.Leu282=
|
|
NM_003597.4:c.897A>G
|
NP_003588.1:p.Leu299=
|
|
XM_005246179.3:c.846A>G
|
XP_005246236.1:p.Leu282=
|
|
NM_003597.5:c.897A>G
MANE Select
|
NP_003588.1:p.Leu299=
|
|
NM_001177716.2:c.846A>G
|
NP_001171187.1:p.Leu282=
|
|
NM_001177718.2:c.846A>G
|
NP_001171189.1:p.Leu282=
|
|