ENST00000696170.1:c.*102G>A
|
ENSP00000512461.1:n.*102G>A
|
|
ENST00000696171.1:c.497G>A
|
ENSP00000512462.1:p.Arg166Gln
|
|
ENST00000696172.1:c.338-2895G>A
|
ENSP00000512463.1:n.338-2895G>A
|
|
ENST00000378588.5:c.593G>A
MANE Select
|
ENSP00000367851.4:p.Arg198Gln
|
|
ENST00000378588.4:c.593G>A
|
ENSP00000367851.4:p.Arg198Gln
|
|
ENST00000465127.1:c.171+370060G>A
|
ENSP00000417050.1:n.171+370060G>A
|
|
NM_000397.3:c.593G>A , LRG_53t1:c.593G>A
|
NP_000388.2:p.Arg198Gln
|
|
XM_011543890.1:c.287G>A
|
XP_011542192.1:p.Arg96Gln
|
|
NM_000397.4:c.593G>A
MANE Select
|
NP_000388.2:p.Arg198Gln
|
|