ENST00000695666.1:n.838C>A
|
|
|
ENST00000695667.1:n.356C>A
|
|
|
ENST00000695668.1:n.2336C>A
|
|
|
ENST00000300692.9:c.351C>A
MANE Select
|
ENSP00000300692.4:p.Leu117=
|
|
ENST00000300692.8:c.351C>A
|
ENSP00000300692.4:p.Leu117=
|
|
ENST00000392884.2:c.275-336C>A
|
ENSP00000376622.2:n.275-336C>A
|
|
ENST00000526561.1:n.80-336C>A
|
|
|
ENST00000529594.5:c.132C>A
|
ENSP00000437335.1:p.Leu44=
|
|
ENST00000534687.5:c.288-336C>A
|
|
|
NM_000732.4:c.351C>A , LRG_37t1:c.351C>A
|
NP_000723.1:p.Leu117=
|
|
NM_001040651.1:c.275-336C>A
|
NP_001035741.1:n.275-336C>A
|
|
NM_001040651.2:c.275-336C>A
|
NP_001035741.1:n.275-336C>A
|
|
NM_000732.6:c.351C>A
MANE Select
|
NP_000723.1:p.Leu117=
|
|