ENST00000696170.1:c.340C>G
|
ENSP00000512461.1:p.Pro114Ala
|
|
ENST00000696171.1:c.390C>G
|
ENSP00000512462.1:p.Asn130Lys
|
|
ENST00000696172.1:c.338-3002C>G
|
ENSP00000512463.1:n.338-3002C>G
|
|
ENST00000378588.5:c.486C>G
MANE Select
|
ENSP00000367851.4:p.Asn162Lys
|
|
ENST00000378588.4:c.486C>G
|
ENSP00000367851.4:p.Asn162Lys
|
|
ENST00000465127.1:c.171+369953C>G
|
ENSP00000417050.1:n.171+369953C>G
|
|
NM_000397.3:c.486C>G , LRG_53t1:c.486C>G
|
NP_000388.2:p.Asn162Lys
|
|
XM_011543890.1:c.180C>G
|
XP_011542192.1:p.Asn60Lys
|
|
NM_000397.4:c.486C>G
MANE Select
|
NP_000388.2:p.Asn162Lys
|
|