|
NM_001017420.3:c.862-2A>G
MANE Select
|
NP_001017420.1:n.862-2A>G
|
|
ENST00000305188.13:c.862-2A>G
MANE Select
|
ENSP00000306999.8:n.862-2A>G
|
|
NM_001017420.2:c.862-2A>G
|
NP_001017420.1:n.862-2A>G
|
|
ENST00000305188.12:c.862-2A>G
|
ENSP00000306999.8:n.862-2A>G
|
|
ENST00000522378.5:c.861+3003A>G
|
ENSP00000428928.1:n.861+3003A>G
|
|
ENST00000523910.1:n.661-2A>G
|
|
|
XM_011544421.1:c.862-2A>G
|
XP_011542723.1:n.862-2A>G
|
|
XM_011544421.2:c.862-2A>G
|
XP_011542723.1:n.862-2A>G
|
|
XM_011544422.1:c.862-2A>G
|
XP_011542724.1:n.862-2A>G
|
|
XM_011544422.2:c.862-2A>G
|
XP_011542724.1:n.862-2A>G
|
|
XR_949378.1:n.946-2A>G
|
|
|
XR_949378.3:n.946-2A>G
|
|
|
XR_949379.1:n.946-2A>G
|
|