ENST00000696170.1:c.*660+111A>G
|
ENSP00000512461.1:n.*660+111A>G
|
|
ENST00000696171.1:c.1055+111A>G
|
ENSP00000512462.1:n.1055+111A>G
|
|
ENST00000378588.5:c.1151+111A>G
MANE Select
|
ENSP00000367851.4:n.1151+111A>G
|
|
ENST00000378588.4:c.1151+111A>G
|
ENSP00000367851.4:n.1151+111A>G
|
|
ENST00000465127.1:c.171+378241A>G
|
ENSP00000417050.1:n.171+378241A>G
|
|
NM_000397.3:c.1151+111A>G , LRG_53t1:c.1151+111A>G
|
NP_000388.2:n.1151+111A>G
|
|
XM_011543890.1:c.845+111A>G
|
XP_011542192.1:n.845+111A>G
|
|
NM_000397.4:c.1151+111A>G
MANE Select
|
NP_000388.2:n.1151+111A>G
|
|