ENST00000696170.1:c.*522A>G
|
ENSP00000512461.1:n.*522A>G
|
|
ENST00000696171.1:c.917A>G
|
ENSP00000512462.1:p.His306Arg
|
|
ENST00000378588.5:c.1013A>G
MANE Select
|
ENSP00000367851.4:p.His338Arg
|
|
ENST00000378588.4:c.1013A>G
|
ENSP00000367851.4:p.His338Arg
|
|
ENST00000465127.1:c.171+377992A>G
|
ENSP00000417050.1:n.171+377992A>G
|
|
ENST00000492288.1:n.438A>G
|
|
|
NM_000397.3:c.1013A>G , LRG_53t1:c.1013A>G
|
NP_000388.2:p.His338Arg
|
|
XM_011543890.1:c.707A>G
|
XP_011542192.1:p.His236Arg
|
|
NM_000397.4:c.1013A>G
MANE Select
|
NP_000388.2:p.His338Arg
|
|