ENST00000371069.5:c.194-14659C>G
MANE Select
|
ENSP00000360108.4:n.194-14659C>G
|
|
ENST00000263441.11:c.-18+4253C>G
|
ENSP00000263441.7:n.-18+4253C>G
|
|
ENST00000371069.4:c.194-14659C>G
|
ENSP00000360108.4:n.194-14659C>G
|
|
ENST00000395325.7:c.23-14659C>G
|
ENSP00000378735.3:n.23-14659C>G
|
|
ENST00000463018.5:n.198+4253C>G
|
|
|
ENST00000483402.1:n.282+4253C>G
|
|
|
ENST00000494710.6:c.116-14659C>G
|
ENSP00000473821.1:n.116-14659C>G
|
|
NM_001256864.1:c.194-14659C>G
|
NP_001243793.1:n.194-14659C>G
|
|
NM_001256865.1:c.-18+4253C>G
|
NP_001243794.1:n.-18+4253C>G
|
|
NM_014787.3:c.23-14659C>G
|
NP_055602.1:n.23-14659C>G
|
|
XM_011542483.1:c.143-14659C>G
|
XP_011540785.1:n.143-14659C>G
|
|
XM_011542484.1:c.116-14659C>G
|
XP_011540786.1:n.116-14659C>G
|
|
XM_011542485.1:c.29-14659C>G
|
XP_011540787.1:n.29-14659C>G
|
|
XM_011542486.1:c.-18+4253C>G
|
XP_011540788.1:n.-18+4253C>G
|
|
XM_011542487.1:c.-18+4253C>G
|
XP_011540789.1:n.-18+4253C>G
|
|
XM_011542488.1:c.-18+4253C>G
|
XP_011540790.1:n.-18+4253C>G
|
|
NM_001256864.2:c.194-14659C>G
MANE Select
|
NP_001243793.1:n.194-14659C>G
|
|
NM_014787.4:c.23-14659C>G
|
NP_055602.1:n.23-14659C>G
|
|
NM_001256865.2:c.-18+4253C>G
|
NP_001243794.1:n.-18+4253C>G
|
|