ENST00000696170.1:c.*549A>G
|
ENSP00000512461.1:n.*549A>G
|
|
ENST00000696171.1:c.944A>G
|
ENSP00000512462.1:p.Glu315Gly
|
|
ENST00000378588.5:c.1040A>G
MANE Select
|
ENSP00000367851.4:p.Glu347Gly
|
|
ENST00000378588.4:c.1040A>G
|
ENSP00000367851.4:p.Glu347Gly
|
|
ENST00000465127.1:c.171+378019A>G
|
ENSP00000417050.1:n.171+378019A>G
|
|
ENST00000492288.1:n.465A>G
|
|
|
NM_000397.3:c.1040A>G , LRG_53t1:c.1040A>G
|
NP_000388.2:p.Glu347Gly
|
|
XM_011543890.1:c.734A>G
|
XP_011542192.1:p.Glu245Gly
|
|
NM_000397.4:c.1040A>G
MANE Select
|
NP_000388.2:p.Glu347Gly
|
|