ENST00000313005.11:c.*478T>C
MANE Select
|
ENSP00000318585.6:n.*478T>C
|
|
ENST00000679585.1:n.2427T>C
|
|
|
ENST00000680271.1:n.1772T>C
|
|
|
ENST00000680681.1:c.*710T>C
|
ENSP00000505419.1:n.*710T>C
|
|
ENST00000680800.1:n.1790T>C
|
|
|
ENST00000680971.1:c.*478T>C
|
ENSP00000506107.1:n.*478T>C
|
|
ENST00000681714.1:n.1245T>C
|
|
|
ENST00000681753.1:n.1187T>C
|
|
|
ENST00000313005.10:c.*478T>C
|
ENSP00000318585.6:n.*478T>C
|
|
ENST00000392937.10:c.*478T>C
|
ENSP00000475405.1:n.*478T>C
|
|
ENST00000528053.5:c.*478T>C
|
ENSP00000431848.1:n.*478T>C
|
|
NM_001207048.1:c.*478T>C
|
NP_001193977.1:n.*478T>C
|
|
NM_001207049.1:c.*478T>C
|
NP_001193978.1:n.*478T>C
|
|
NM_012104.4:c.*478T>C
|
NP_036236.1:n.*478T>C
|
|
NM_138971.3:c.*478T>C
|
NP_620427.1:n.*478T>C
|
|
NM_138972.3:c.*478T>C
|
NP_620428.1:n.*478T>C
|
|
NM_138973.3:c.*478T>C
|
NP_620429.1:n.*478T>C
|
|
NM_001207048.2:c.*478T>C
|
NP_001193977.1:n.*478T>C
|
|
NM_001207049.2:c.*478T>C
|
NP_001193978.1:n.*478T>C
|
|
NM_001207048.3:c.*478T>C
|
NP_001193977.1:n.*478T>C
|
|
NM_001207049.3:c.*478T>C
|
NP_001193978.1:n.*478T>C
|
|
NM_012104.6:c.*478T>C
MANE Select
|
NP_036236.1:n.*478T>C
|
|
NM_138971.4:c.*478T>C
|
NP_620427.1:n.*478T>C
|
|
NM_138972.4:c.*478T>C
|
NP_620428.1:n.*478T>C
|
|
NM_138973.4:c.*478T>C
|
NP_620429.1:n.*478T>C
|
|