ENST00000695666.1:n.852T>G
|
|
|
ENST00000695667.1:n.370T>G
|
|
|
ENST00000695668.1:n.2350T>G
|
|
|
ENST00000300692.9:c.365T>G
MANE Select
|
ENSP00000300692.4:p.Val122Gly
|
|
ENST00000300692.8:c.365T>G
|
ENSP00000300692.4:p.Val122Gly
|
|
ENST00000392884.2:c.275-322T>G
|
ENSP00000376622.2:n.275-322T>G
|
|
ENST00000526561.1:n.80-322T>G
|
|
|
ENST00000529594.5:c.146T>G
|
ENSP00000437335.1:p.Val49Gly
|
|
ENST00000534687.5:c.288-322T>G
|
|
|
NM_000732.4:c.365T>G , LRG_37t1:c.365T>G
|
NP_000723.1:p.Val122Gly
|
|
NM_001040651.1:c.275-322T>G
|
NP_001035741.1:n.275-322T>G
|
|
NM_001040651.2:c.275-322T>G
|
NP_001035741.1:n.275-322T>G
|
|
NM_000732.6:c.365T>G
MANE Select
|
NP_000723.1:p.Val122Gly
|
|