NM_000732.6:c.444C>G
MANE Select
|
NP_000723.1:p.Val148=
|
ENST00000300692.9:c.444C>G
MANE Select
|
ENSP00000300692.4:p.Val148=
|
NM_000732.4:c.444C>G , LRG_37t1:c.444C>G
|
NP_000723.1:p.Val148=
|
NM_001040651.1:c.312C>G
|
NP_001035741.1:p.Val104=
|
NM_001040651.2:c.312C>G
|
NP_001035741.1:p.Val104=
|
ENST00000300692.8:c.444C>G
|
ENSP00000300692.4:p.Val148=
|
ENST00000392884.2:c.312C>G
|
ENSP00000376622.2:p.Val104=
|
ENST00000526561.1:n.117C>G
|
|
ENST00000529594.5:c.225C>G
|
ENSP00000437335.1:p.Val75=
|
ENST00000534687.5:c.325C>G
|
|
ENST00000695666.1:n.1211C>G
|
|
ENST00000695667.1:n.729C>G
|
|