ENST00000309755.9:c.1180G>T
MANE Select
|
ENSP00000312397.4:p.Asp394Tyr
|
|
ENST00000309755.8:c.1180G>T
|
ENSP00000312397.4:p.Asp394Tyr
|
|
ENST00000502381.1:n.767G>T
|
|
|
ENST00000504208.5:c.*335-10555G>T
|
ENSP00000423585.1:n.*335-10555G>T
|
|
ENST00000505853.1:c.1060G>T
|
ENSP00000426173.1:p.Asp354Tyr
|
|
ENST00000506491.5:c.934G>T
|
ENSP00000424828.1:p.Asp312Tyr
|
|
ENST00000506873.5:n.805G>T
|
|
|
ENST00000508657.5:c.1084G>T
|
ENSP00000422099.1:p.Asp362Tyr
|
|
NM_001257194.1:c.1084G>T
|
NP_001244123.1:p.Asp362Tyr
|
|
NM_001257195.1:c.934G>T
|
NP_001244124.1:p.Asp312Tyr
|
|
NM_017415.2:c.1180G>T
|
NP_059111.2:p.Asp394Tyr
|
|
NM_017415.3:c.1180G>T
MANE Select
|
NP_059111.2:p.Asp394Tyr
|
|
NM_001257195.2:c.934G>T
|
NP_001244124.1:p.Asp312Tyr
|
|