ENST00000366669.9:c.1823T>G
MANE Select
|
ENSP00000355629.4:p.Val608Gly
|
|
ENST00000366668.7:c.1820T>G
|
ENSP00000355628.3:p.Val607Gly
|
|
ENST00000366669.8:c.1823T>G
|
ENSP00000355629.4:p.Val608Gly
|
|
ENST00000468893.6:c.*1681T>G
|
ENSP00000476305.1:n.*1681T>G
|
|
ENST00000478710.1:n.82T>G
|
|
|
ENST00000490900.1:n.602T>G
|
|
|
ENST00000534989.1:c.1646T>G
|
ENSP00000440349.1:p.Val549Gly
|
|
NM_001145036.1:c.1820T>G
|
NP_001138508.1:p.Val607Gly
|
|
NM_007357.2:c.1823T>G
|
NP_031383.1:p.Val608Gly
|
|
NM_007357.3:c.1823T>G
MANE Select
|
NP_031383.1:p.Val608Gly
|
|
NM_001145036.2:c.1820T>G
|
NP_001138508.1:p.Val607Gly
|
|