|
NM_004984.4:c.2987A>G
MANE Select
|
NP_004975.2:p.Asp996Gly
|
|
ENST00000455537.7:c.2987A>G
MANE Select
|
ENSP00000408979.2:p.Asp996Gly
|
|
NM_001354705.1:c.2720A>G
|
NP_001341634.1:p.Asp907Gly
|
|
NM_001354705.2:c.2720A>G
|
NP_001341634.1:p.Asp907Gly
|
|
NM_004984.2:c.2987A>G
|
NP_004975.2:p.Asp996Gly
|
|
NM_004984.3:c.2987A>G
|
NP_004975.2:p.Asp996Gly
|
|
ENST00000286452.5:c.2720A>G
|
ENSP00000286452.5:p.Asp907Gly
|
|
ENST00000455537.6:c.2987A>G
|
ENSP00000408979.2:p.Asp996Gly
|
|
ENST00000552227.1:n.270A>G
|
|
|
ENST00000674619.1:c.3008A>G
|
ENSP00000502270.1:p.Asp1003Gly
|
|
ENST00000675697.1:c.78A>G
|
|
|
ENST00000675737.1:n.391A>G
|
|
|
ENST00000675882.1:n.2510A>G
|
|
|
ENST00000675929.1:n.1545A>G
|
|
|
ENST00000676055.1:c.78A>G
|
|
|
ENST00000676437.1:c.12A>G
|
|
|
ENST00000676457.1:c.2882A>G
|
ENSP00000501588.1:p.Asp961Gly
|
|
XR_002957324.1:n.3220A>G
|
|