ENST00000388958.8:c.1187G>T
|
ENSP00000373610.3:p.Gly396Val
|
|
ENST00000646100.2:c.1187G>T
MANE Select
|
ENSP00000496564.2:p.Gly396Val
|
|
ENST00000647277.1:c.*1G>T
|
ENSP00000495594.1:n.*1G>T
|
|
ENST00000286149.8:c.1229G>T
|
ENSP00000286149.4:p.Gly410Val
|
|
ENST00000388956.8:c.950G>T
|
ENSP00000373608.4:p.Gly317Val
|
|
ENST00000388957.3:c.215G>T
|
ENSP00000373609.3:p.Gly72Val
|
|
ENST00000388958.7:c.1187G>T
|
ENSP00000373610.3:p.Gly396Val
|
|
ENST00000563871.5:n.407G>T
|
|
|
NM_001161683.1:c.950G>T
|
NP_001155155.1:p.Gly317Val
|
|
NM_144672.3:c.1187G>T
|
NP_653273.3:p.Gly396Val
|
|
NM_170664.2:c.215G>T
|
NP_733764.1:p.Gly72Val
|
|
XM_011545747.1:c.1187G>T
|
XP_011544049.1:p.Gly396Val
|
|
XM_011545748.1:c.56G>T
|
XP_011544050.1:p.Gly19Val
|
|
NM_144672.4:c.1187G>T
MANE Select
|
NP_653273.3:p.Gly396Val
|
|
XM_011545748.2:c.56G>T
|
XP_011544050.2:p.Gly19Val
|
|
XR_002957775.1:n.282G>T
|
|
|
NM_001161683.2:c.950G>T
|
NP_001155155.1:p.Gly317Val
|
|
NM_170664.3:c.215G>T
|
NP_733764.1:p.Gly72Val
|
|