ENST00000695666.1:n.813T>G
|
|
|
ENST00000695667.1:n.331T>G
|
|
|
ENST00000695668.1:n.2311T>G
|
|
|
ENST00000300692.9:c.326T>G
MANE Select
|
ENSP00000300692.4:p.Val109Gly
|
|
ENST00000300692.8:c.326T>G
|
ENSP00000300692.4:p.Val109Gly
|
|
ENST00000392884.2:c.275-361T>G
|
ENSP00000376622.2:n.275-361T>G
|
|
ENST00000526561.1:n.80-361T>G
|
|
|
ENST00000529594.5:c.107T>G
|
ENSP00000437335.1:p.Val36Gly
|
|
ENST00000534687.5:c.288-361T>G
|
|
|
NM_000732.4:c.326T>G , LRG_37t1:c.326T>G
|
NP_000723.1:p.Val109Gly
|
|
NM_001040651.1:c.275-361T>G
|
NP_001035741.1:n.275-361T>G
|
|
NM_001040651.2:c.275-361T>G
|
NP_001035741.1:n.275-361T>G
|
|
NM_000732.6:c.326T>G
MANE Select
|
NP_000723.1:p.Val109Gly
|
|