ENST00000216075.11:c.822C>G
MANE Select
|
ENSP00000216075.6:p.Leu274=
|
|
ENST00000216075.10:c.822C>G
|
ENSP00000216075.6:p.Leu274=
|
|
ENST00000395732.7:c.808C>G
|
ENSP00000379081.3:p.His270Asp
|
|
ENST00000395733.7:c.691C>G
|
ENSP00000379082.3:p.His231Asp
|
|
ENST00000451761.1:c.762C>G
|
ENSP00000409894.1:p.Leu254=
|
|
NM_017584.5:c.822C>G
|
NP_060054.4:p.Leu274=
|
|
XM_005261925.3:c.684C>G
|
XP_005261982.1:p.Leu228=
|
|
XR_244455.2:n.3318C>G
|
|
|
XM_005261925.4:c.684C>G
|
XP_005261982.1:p.Leu228=
|
|
NM_017584.6:c.822C>G
MANE Select
|
NP_060054.4:p.Leu274=
|
|