ENST00000324001.8:c.2256G=
MANE Select
|
ENSP00000326018.6:p.Glu752=
|
|
ENST00000673881.1:c.1839G=
|
ENSP00000501070.1:p.Glu613=
|
|
ENST00000674005.2:c.2541G=
|
ENSP00000501261.1:p.Glu847=
|
|
ENST00000674773.1:c.1839G=
|
ENSP00000502579.1:p.Glu613=
|
|
ENST00000675517.1:c.2131G=
|
|
|
ENST00000676076.1:c.2117G=
|
|
|
ENST00000676260.1:c.2218G=
|
|
|
ENST00000676316.1:c.2143G=
|
|
|
ENST00000291825.11:c.*2461G=
|
ENSP00000291825.6:n.*2461G=
|
|
ENST00000324001.7:c.2256G=
|
ENSP00000326018.6:p.Glu752=
|
|
NM_020956.2:c.*2461G= , LRG_265t1:c.*2461G=
|
NP_066007.1:n.*2461G=
|
|
NM_181882.2:c.2256G= , LRG_265t2:c.2256G=
|
NP_870998.2:p.Glu752=
|
|
XM_011527171.1:c.2256G=
|
XP_011525473.1:p.Glu752=
|
|
XM_011527171.2:c.2256G=
|
XP_011525473.1:p.Glu752=
|
|
XM_017027046.1:c.2154G=
|
XP_016882535.1:p.Glu718=
|
|
XM_017027047.1:c.2154G=
|
XP_016882536.1:p.Glu718=
|
|
NM_181882.3:c.2256G=
MANE Select
|
NP_870998.2:p.Glu752=
|
|