ENST00000287152.12:c.2181-1613A>G
MANE Select
|
ENSP00000287152.7:n.2181-1613A>G
|
|
ENST00000229913.9:c.534-1613A>G
|
ENSP00000229913.5:n.534-1613A>G
|
|
ENST00000287152.11:c.2181-1613A>G
|
ENSP00000287152.7:n.2181-1613A>G
|
|
ENST00000394362.5:c.534-2350A>G
|
ENSP00000377889.1:n.534-2350A>G
|
|
ENST00000458470.5:c.1856-2350A>G
|
|
|
ENST00000538893.5:c.534-1613A>G
|
ENSP00000441435.2:n.534-1613A>G
|
|
NM_001289020.1:c.2130-1613A>G
|
NP_001275949.1:n.2130-1613A>G
|
|
NM_001289021.1:c.2013-1613A>G
|
NP_001275950.1:n.2013-1613A>G
|
|
NM_001289024.1:c.534-1613A>G
|
NP_001275953.1:n.534-1613A>G
|
|
NM_145027.4:c.2181-1613A>G
|
NP_659464.3:n.2181-1613A>G
|
|
XM_005248904.3:c.2181-1613A>G
|
XP_005248961.1:n.2181-1613A>G
|
|
XM_011514357.1:c.2181-2350A>G
|
XP_011512659.1:n.2181-2350A>G
|
|
XM_011514358.1:c.2181-1613A>G
|
XP_011512660.1:n.2181-1613A>G
|
|
XM_011514359.1:c.2181-2350A>G
|
XP_011512661.1:n.2181-2350A>G
|
|
XM_011514360.1:c.1554-1613A>G
|
XP_011512662.1:n.1554-1613A>G
|
|
NM_001289020.2:c.2130-1613A>G
|
NP_001275949.1:n.2130-1613A>G
|
|
NM_001289021.2:c.2013-1613A>G
|
NP_001275950.1:n.2013-1613A>G
|
|
NM_001289024.2:c.534-1613A>G
|
NP_001275953.1:n.534-1613A>G
|
|
NM_001351566.1:c.534-1613A>G
|
NP_001338495.1:n.534-1613A>G
|
|
NM_145027.5:c.2181-1613A>G
|
NP_659464.3:n.2181-1613A>G
|
|
XM_005248904.4:c.2181-1613A>G
|
XP_005248961.1:n.2181-1613A>G
|
|
XM_011514357.3:c.2181-2350A>G
|
XP_011512659.1:n.2181-2350A>G
|
|
XM_011514358.3:c.2181-1613A>G
|
XP_011512660.1:n.2181-1613A>G
|
|
XM_011514359.3:c.2181-2350A>G
|
XP_011512661.1:n.2181-2350A>G
|
|
XM_017010427.1:c.1872-1613A>G
|
XP_016865916.1:n.1872-1613A>G
|
|
XM_017010428.1:c.1536-1613A>G
|
XP_016865917.1:n.1536-1613A>G
|
|
NM_145027.6:c.2181-1613A>G
MANE Select
|
NP_659464.3:n.2181-1613A>G
|
|
NM_001289020.3:c.2130-1613A>G
|
NP_001275949.1:n.2130-1613A>G
|
|
NM_001289021.3:c.2013-1613A>G
|
NP_001275950.1:n.2013-1613A>G
|
|
NM_001289024.3:c.534-1613A>G
|
NP_001275953.1:n.534-1613A>G
|
|
NM_001351566.2:c.534-1613A>G
|
NP_001338495.1:n.534-1613A>G
|
|