ENST00000681320.1:c.7971C>T
MANE Select
|
ENSP00000506558.1:p.His2657=
|
|
ENST00000328333.12:c.7971C>T
|
ENSP00000332371.8:p.His2657=
|
|
ENST00000459756.5:n.794C>T
|
|
|
ENST00000487017.5:n.4610C>T
|
|
|
NM_000094.3:c.7971C>T , LRG_286t1:c.7971C>T
|
NP_000085.1:p.His2657=
|
|
XM_011533336.1:c.7998C>T
|
XP_011531638.1:p.His2666=
|
|
XM_011533337.1:c.7971C>T
|
XP_011531639.1:p.His2657=
|
|
XM_011533338.1:c.7938C>T
|
XP_011531640.1:p.His2646=
|
|
XR_940369.1:n.8034C>T
|
|
|
XR_940370.1:n.8034C>T
|
|
|
XR_940371.1:n.8034C>T
|
|
|
XM_017005688.1:c.7911C>T
|
XP_016861177.1:p.His2637=
|
|
XR_001740003.1:n.8007C>T
|
|
|
XR_001740004.1:n.8007C>T
|
|
|
XR_001740005.1:n.8007C>T
|
|
|
NM_000094.4:c.7971C>T
MANE Select
|
NP_000085.1:p.His2657=
|
|