ENST00000338758.12:c.1018+1384A>T
MANE Select
|
ENSP00000342492.6:n.1018+1384A>T
|
|
ENST00000338758.11:c.1018+1384A>T
|
ENSP00000342492.6:n.1018+1384A>T
|
|
ENST00000404989.1:c.907+1384A>T
|
ENSP00000384353.1:n.907+1384A>T
|
|
ENST00000406477.7:c.1117+1384A>T
|
ENSP00000384515.3:n.1117+1384A>T
|
|
ENST00000484345.1:n.191+1384A>T
|
|
|
ENST00000619710.4:c.793+1384A>T
|
ENSP00000482511.1:n.793+1384A>T
|
|
NM_001003828.2:c.1117+1384A>T
|
NP_001003828.1:n.1117+1384A>T
|
|
NM_001243385.1:c.907+1384A>T
|
NP_001230314.1:n.907+1384A>T
|
|
NM_001243386.1:c.793+1384A>T
|
NP_001230315.1:n.793+1384A>T
|
|
NM_013327.4:c.1018+1384A>T
|
NP_037459.2:n.1018+1384A>T
|
|
XM_005261596.1:c.862+1384A>T
|
XP_005261653.1:n.862+1384A>T
|
|
XM_017028792.2:c.949+1384A>T
|
XP_016884281.1:n.949+1384A>T
|
|
XM_024452235.1:c.1072+1384A>T
|
XP_024308003.1:n.1072+1384A>T
|
|
XM_024452236.1:c.1048+1384A>T
|
XP_024308004.1:n.1048+1384A>T
|
|
XM_024452237.1:c.907+1384A>T
|
XP_024308005.1:n.907+1384A>T
|
|
NM_001003828.3:c.1117+1384A>T
|
NP_001003828.1:n.1117+1384A>T
|
|
NM_001243385.2:c.907+1384A>T
|
NP_001230314.1:n.907+1384A>T
|
|
NM_001243386.2:c.793+1384A>T
|
NP_001230315.1:n.793+1384A>T
|
|
NM_013327.5:c.1018+1384A>T
MANE Select
|
NP_037459.2:n.1018+1384A>T
|
|