ENST00000696170.1:c.*105G>C
|
ENSP00000512461.1:n.*105G>C
|
|
ENST00000696171.1:c.500G>C
|
ENSP00000512462.1:p.Arg167Thr
|
|
ENST00000696172.1:c.338-2892G>C
|
ENSP00000512463.1:n.338-2892G>C
|
|
ENST00000378588.5:c.596G>C
MANE Select
|
ENSP00000367851.4:p.Arg199Thr
|
|
ENST00000378588.4:c.596G>C
|
ENSP00000367851.4:p.Arg199Thr
|
|
ENST00000465127.1:c.171+370063G>C
|
ENSP00000417050.1:n.171+370063G>C
|
|
NM_000397.3:c.596G>C , LRG_53t1:c.596G>C
|
NP_000388.2:p.Arg199Thr
|
|
XM_011543890.1:c.290G>C
|
XP_011542192.1:p.Arg97Thr
|
|
NM_000397.4:c.596G>C
MANE Select
|
NP_000388.2:p.Arg199Thr
|
|