ENST00000309755.9:c.922G>T
MANE Select
|
ENSP00000312397.4:p.Gly308Cys
|
|
ENST00000309755.8:c.922G>T
|
ENSP00000312397.4:p.Gly308Cys
|
|
ENST00000502381.1:n.509G>T
|
|
|
ENST00000504208.5:c.*335-11522G>T
|
ENSP00000423585.1:n.*335-11522G>T
|
|
ENST00000505853.1:c.802G>T
|
ENSP00000426173.1:p.Gly268Cys
|
|
ENST00000506491.5:c.676G>T
|
ENSP00000424828.1:p.Gly226Cys
|
|
ENST00000506873.5:n.547G>T
|
|
|
ENST00000508657.5:c.826G>T
|
ENSP00000422099.1:p.Gly276Cys
|
|
NM_001257194.1:c.826G>T
|
NP_001244123.1:p.Gly276Cys
|
|
NM_001257195.1:c.676G>T
|
NP_001244124.1:p.Gly226Cys
|
|
NM_017415.2:c.922G>T
|
NP_059111.2:p.Gly308Cys
|
|
NM_017415.3:c.922G>T
MANE Select
|
NP_059111.2:p.Gly308Cys
|
|
NM_001257195.2:c.676G>T
|
NP_001244124.1:p.Gly226Cys
|
|