ENST00000313005.11:c.*3389C>G
(BACE1)
MANE Select
|
ENSP00000318585.6:n.*3389C>G
|
|
ENST00000300650.9:c.*1026G>C
(RNF214)
MANE Select
|
ENSP00000300650.4:n.*1026G>C
|
|
ENST00000679585.1:n.5338C>G
(BACE1)
|
|
|
ENST00000680271.1:n.4683C>G
(BACE1)
|
|
|
ENST00000680800.1:n.4701C>G
(BACE1)
|
|
|
ENST00000680971.1:c.*3389C>G
(BACE1)
|
ENSP00000506107.1:n.*3389C>G
|
|
ENST00000313005.10:c.*3389C>G
(BACE1)
|
ENSP00000318585.6:n.*3389C>G
|
|
ENST00000392937.10:c.*3389C>G
(BACE1)
|
ENSP00000475405.1:n.*3389C>G
|
|
ENST00000530849.1:c.*1026G>C
(RNF214)
|
ENSP00000432903.1:n.*1026G>C
|
|
NM_001207048.1:c.*3389C>G
(BACE1)
|
NP_001193977.1:n.*3389C>G
|
|
NM_001207049.1:c.*3389C>G
(BACE1)
|
NP_001193978.1:n.*3389C>G
|
|
NM_012104.4:c.*3389C>G
(BACE1)
|
NP_036236.1:n.*3389C>G
|
|
NM_138971.3:c.*3389C>G
(BACE1)
|
NP_620427.1:n.*3389C>G
|
|
NM_138972.3:c.*3389C>G
(BACE1)
|
NP_620428.1:n.*3389C>G
|
|
NM_138973.3:c.*3389C>G
(BACE1)
|
NP_620429.1:n.*3389C>G
|
|
NM_207343.4:c.*1026G>C
(RNF214)
MANE Select
|
NP_997226.2:n.*1026G>C
|
|
NM_001207048.2:c.*3389C>G
(BACE1)
|
NP_001193977.1:n.*3389C>G
|
|
NM_001207049.2:c.*3389C>G
(BACE1)
|
NP_001193978.1:n.*3389C>G
|
|
NM_001077239.2:c.*1026G>C
(RNF214)
|
NP_001070707.1:n.*1026G>C
|
|
NM_001207048.3:c.*3389C>G
(BACE1)
|
NP_001193977.1:n.*3389C>G
|
|
NM_001207049.3:c.*3389C>G
(BACE1)
|
NP_001193978.1:n.*3389C>G
|
|
NM_001278249.2:c.*1026G>C
(RNF214)
|
NP_001265178.1:n.*1026G>C
|
|
NM_012104.6:c.*3389C>G
(BACE1)
MANE Select
|
NP_036236.1:n.*3389C>G
|
|
NM_138971.4:c.*3389C>G
(BACE1)
|
NP_620427.1:n.*3389C>G
|
|
NM_138972.4:c.*3389C>G
(BACE1)
|
NP_620428.1:n.*3389C>G
|
|
NM_138973.4:c.*3389C>G
(BACE1)
|
NP_620429.1:n.*3389C>G
|
|