ENST00000696170.1:c.*513T>G
|
ENSP00000512461.1:n.*513T>G
|
|
ENST00000696171.1:c.908T>G
|
ENSP00000512462.1:p.Leu303Arg
|
|
ENST00000378588.5:c.1004T>G
MANE Select
|
ENSP00000367851.4:p.Leu335Arg
|
|
ENST00000378588.4:c.1004T>G
|
ENSP00000367851.4:p.Leu335Arg
|
|
ENST00000465127.1:c.171+377983T>G
|
ENSP00000417050.1:n.171+377983T>G
|
|
ENST00000492288.1:n.429T>G
|
|
|
NM_000397.3:c.1004T>G , LRG_53t1:c.1004T>G
|
NP_000388.2:p.Leu335Arg
|
|
XM_011543890.1:c.698T>G
|
XP_011542192.1:p.Leu233Arg
|
|
NM_000397.4:c.1004T>G
MANE Select
|
NP_000388.2:p.Leu335Arg
|
|