ENST00000350051.8:c.340-128G>T
MANE Select
|
ENSP00000324180.4:n.340-128G>T
|
|
ENST00000301633.8:c.409-128G>T
|
ENSP00000301633.3:n.409-128G>T
|
|
ENST00000350051.7:c.340-128G>T
|
ENSP00000324180.4:n.340-128G>T
|
|
ENST00000374948.6:c.222-128G>T
|
ENSP00000364086.1:n.222-128G>T
|
|
ENST00000589892.1:n.356-128G>T
|
|
|
ENST00000590925.6:c.*142-128G>T
|
ENSP00000467336.1:n.*142-128G>T
|
|
NM_001012270.1:c.222-128G>T
|
NP_001012270.1:n.222-128G>T
|
|
NM_001012271.1:c.409-128G>T
|
NP_001012271.1:n.409-128G>T
|
|
NM_001168.2:c.340-128G>T
|
NP_001159.2:n.340-128G>T
|
|
XR_243654.3:n.542-128G>T
|
|
|
XR_934452.1:n.611-128G>T
|
|
|
XR_243654.5:n.542-128G>T
|
|
|
XR_934452.3:n.611-128G>T
|
|
|
NM_001168.3:c.340-128G>T
MANE Select
|
NP_001159.2:n.340-128G>T
|
|
NM_001012270.2:c.222-128G>T
|
NP_001012270.1:n.222-128G>T
|
|
NM_001012271.2:c.409-128G>T
|
NP_001012271.1:n.409-128G>T
|
|