ENST00000469834.2:n.697A>G
|
|
|
ENST00000493114.2:c.492+117A>G
|
ENSP00000436094.2:n.492+117A>G
|
|
ENST00000696871.1:c.492+117A>G
|
ENSP00000512940.1:n.492+117A>G
|
|
ENST00000696872.1:c.552+117A>G
|
ENSP00000512941.1:n.552+117A>G
|
|
ENST00000696873.1:c.57+117A>G
|
ENSP00000512942.1:n.57+117A>G
|
|
ENST00000380956.9:c.492+117A>G
MANE Select
|
ENSP00000370343.4:n.492+117A>G
|
|
ENST00000380956.8:c.492+117A>G
|
ENSP00000370343.4:n.492+117A>G
|
|
ENST00000468485.5:n.451A>G
|
|
|
ENST00000493114.1:c.492+117A>G
|
ENSP00000436094.1:n.492+117A>G
|
|
ENST00000495137.5:n.318+117A>G
|
|
|
NM_001195286.1:c.492+117A>G
|
NP_001182215.1:n.492+117A>G
|
|
NM_002460.3:c.492+117A>G
|
NP_002451.2:n.492+117A>G
|
|
NR_046000.2:n.618+117A>G
|
|
|
XM_006715090.1:c.492+117A>G
|
XP_006715153.1:n.492+117A>G
|
|
XM_006715090.2:c.492+117A>G
|
XP_006715153.1:n.492+117A>G
|
|
NM_002460.4:c.492+117A>G
MANE Select
|
NP_002451.2:n.492+117A>G
|
|
NM_001195286.2:c.492+117A>G
|
NP_001182215.1:n.492+117A>G
|
|
NR_046000.3:n.605+117A>G
|
|
|