ENST00000358102.8:c.*171T>C
MANE Select
|
ENSP00000350815.3:n.*171T>C
|
|
ENST00000342437.8:c.*509T>C
|
ENSP00000343907.4:n.*509T>C
|
|
ENST00000344721.8:c.*171T>C
|
ENSP00000341390.4:n.*171T>C
|
|
ENST00000358102.7:c.*171T>C
|
ENSP00000350815.3:n.*171T>C
|
|
ENST00000512865.5:c.*171T>C
|
ENSP00000423510.1:n.*171T>C
|
|
ENST00000625323.2:c.*171T>C
|
ENSP00000486719.1:n.*171T>C
|
|
NM_000901.4:c.*171T>C
|
NP_000892.2:n.*171T>C
|
|
NM_001166104.1:c.*171T>C
|
NP_001159576.1:n.*171T>C
|
|
XM_011531975.1:c.*171T>C
|
XP_011530277.1:n.*171T>C
|
|
XM_011531976.1:c.*171T>C
|
XP_011530278.1:n.*171T>C
|
|
XM_011531977.1:c.*171T>C
|
XP_011530279.1:n.*171T>C
|
|
NM_001354819.1:c.*171T>C
|
NP_001341748.1:n.*171T>C
|
|
NR_148974.1:n.2993T>C
|
|
|
NM_000901.5:c.*171T>C
MANE Select
|
NP_000892.2:n.*171T>C
|
|
NM_001166104.2:c.*171T>C
|
NP_001159576.1:n.*171T>C
|
|
NR_148974.2:n.2887T>C
|
|
|