ENST00000696170.1:c.*511G>C
|
ENSP00000512461.1:n.*511G>C
|
|
ENST00000696171.1:c.906G>C
|
ENSP00000512462.1:p.Lys302Asn
|
|
ENST00000378588.5:c.1002G>C
MANE Select
|
ENSP00000367851.4:p.Lys334Asn
|
|
ENST00000378588.4:c.1002G>C
|
ENSP00000367851.4:p.Lys334Asn
|
|
ENST00000465127.1:c.171+377981G>C
|
ENSP00000417050.1:n.171+377981G>C
|
|
ENST00000492288.1:n.427G>C
|
|
|
NM_000397.3:c.1002G>C , LRG_53t1:c.1002G>C
|
NP_000388.2:p.Lys334Asn
|
|
XM_011543890.1:c.696G>C
|
XP_011542192.1:p.Lys232Asn
|
|
NM_000397.4:c.1002G>C
MANE Select
|
NP_000388.2:p.Lys334Asn
|
|