ENST00000227322.8:c.892-100G>T
MANE Select
|
ENSP00000227322.3:n.892-100G>T
|
|
ENST00000227322.7:c.892-100G>T
|
ENSP00000227322.3:n.892-100G>T
|
|
ENST00000429220.5:c.671-100G>T
|
|
|
ENST00000444935.5:c.891-100G>T
|
|
|
ENST00000449430.1:c.404-100G>T
|
ENSP00000415505.1:n.404-100G>T
|
|
NM_003904.3:c.892-100G>T
|
NP_003895.1:n.892-100G>T
|
|
NM_001317086.1:c.730-100G>T
|
NP_001304015.1:n.730-100G>T
|
|
NM_003904.4:c.892-100G>T
|
NP_003895.1:n.892-100G>T
|
|
XR_001748023.2:n.2220-100G>T
|
|
|
NM_003904.5:c.892-100G>T
MANE Select
|
NP_003895.1:n.892-100G>T
|
|
NM_001317086.2:c.730-100G>T
|
NP_001304015.1:n.730-100G>T
|
|