ENST00000681320.1:c.8386C>T
MANE Select
|
ENSP00000506558.1:p.Gln2796Ter
|
|
ENST00000328333.12:c.8386C>T
|
ENSP00000332371.8:p.Gln2796Ter
|
|
ENST00000487017.5:n.5025C>T
|
|
|
NM_000094.3:c.8386C>T , LRG_286t1:c.8386C>T
|
NP_000085.1:p.Gln2796Ter
|
|
XM_011533336.1:c.8413C>T
|
XP_011531638.1:p.Gln2805Ter
|
|
XM_011533337.1:c.8386C>T
|
XP_011531639.1:p.Gln2796Ter
|
|
XM_011533338.1:c.8353C>T
|
XP_011531640.1:p.Gln2785Ter
|
|
XR_940369.1:n.8449C>T
|
|
|
XR_940370.1:n.8449C>T
|
|
|
XR_940371.1:n.8449C>T
|
|
|
XM_017005688.1:c.8326C>T
|
XP_016861177.1:p.Gln2776Ter
|
|
XR_001740003.1:n.8422C>T
|
|
|
XR_001740004.1:n.8422C>T
|
|
|
XR_001740005.1:n.8422C>T
|
|
|
NM_000094.4:c.8386C>T
MANE Select
|
NP_000085.1:p.Gln2796Ter
|
|