ENST00000681320.1:c.7992T>G
MANE Select
|
ENSP00000506558.1:p.Pro2664=
|
|
ENST00000328333.12:c.7992T>G
|
ENSP00000332371.8:p.Pro2664=
|
|
ENST00000487017.5:n.4631T>G
|
|
|
NM_000094.3:c.7992T>G , LRG_286t1:c.7992T>G
|
NP_000085.1:p.Pro2664=
|
|
XM_011533336.1:c.8019T>G
|
XP_011531638.1:p.Pro2673=
|
|
XM_011533337.1:c.7992T>G
|
XP_011531639.1:p.Pro2664=
|
|
XM_011533338.1:c.7959T>G
|
XP_011531640.1:p.Pro2653=
|
|
XR_940369.1:n.8055T>G
|
|
|
XR_940370.1:n.8055T>G
|
|
|
XR_940371.1:n.8055T>G
|
|
|
XM_017005688.1:c.7932T>G
|
XP_016861177.1:p.Pro2644=
|
|
XR_001740003.1:n.8028T>G
|
|
|
XR_001740004.1:n.8028T>G
|
|
|
XR_001740005.1:n.8028T>G
|
|
|
NM_000094.4:c.7992T>G
MANE Select
|
NP_000085.1:p.Pro2664=
|
|