ENST00000676179.1:c.*2039T>C
MANE Select
|
ENSP00000502065.1:n.*2039T>C
|
|
ENST00000377081.5:c.*224T>C
|
ENSP00000366284.1:n.*224T>C
|
|
ENST00000377086.5:c.*2039T>C
|
ENSP00000366290.1:n.*2039T>C
|
|
ENST00000620295.2:c.5654T>C
|
ENSP00000478500.1:n.5654T>C
|
|
ENST00000622724.3:c.5618T>C
|
ENSP00000480063.1:n.5618T>C
|
|
NM_015074.3:c.*2039T>C , LRG_252t1:c.*2039T>C
|
NP_055889.2:n.*2039T>C
|
|
NM_001365951.1:c.*2039T>C
|
NP_001352880.1:n.*2039T>C
|
|
NM_001365952.1:c.*2039T>C
|
NP_001352881.1:n.*2039T>C
|
|
NM_001365951.3:c.*2039T>C
MANE Select
|
NP_001352880.1:n.*2039T>C
|
|