ENST00000696170.1:c.*177G>A
|
ENSP00000512461.1:n.*177G>A
|
|
ENST00000696171.1:c.572G>A
|
ENSP00000512462.1:p.Gly191Glu
|
|
ENST00000696172.1:c.338-2820G>A
|
ENSP00000512463.1:n.338-2820G>A
|
|
ENST00000378588.5:c.668G>A
MANE Select
|
ENSP00000367851.4:p.Gly223Glu
|
|
ENST00000378588.4:c.668G>A
|
ENSP00000367851.4:p.Gly223Glu
|
|
ENST00000465127.1:c.171+370135G>A
|
ENSP00000417050.1:n.171+370135G>A
|
|
NM_000397.3:c.668G>A , LRG_53t1:c.668G>A
|
NP_000388.2:p.Gly223Glu
|
|
XM_011543890.1:c.362G>A
|
XP_011542192.1:p.Gly121Glu
|
|
NM_000397.4:c.668G>A
MANE Select
|
NP_000388.2:p.Gly223Glu
|
|