ENST00000253122.10:c.1265T>G
MANE Select
|
ENSP00000253122.5:p.Val422Gly
|
|
ENST00000253122.9:c.1265T>G
|
ENSP00000253122.5:p.Val422Gly
|
|
ENST00000413787.1:c.258-64T>G
|
ENSP00000400463.1:n.258-64T>G
|
|
ENST00000430077.6:c.920T>G
|
ENSP00000403041.2:p.Val307Gly
|
|
ENST00000442457.1:c.319T>G
|
|
|
ENST00000457723.1:c.242T>G
|
ENSP00000394742.1:p.Val81Gly
|
|
ENST00000485324.1:n.1410T>G
|
|
|
NM_001142805.1:c.1235T>G
|
NP_001136277.1:p.Val412Gly
|
|
NM_001142806.1:c.920T>G
|
NP_001136278.1:p.Val307Gly
|
|
NM_005629.3:c.1265T>G
|
NP_005620.1:p.Val422Gly
|
|
NM_005629.4:c.1265T>G
MANE Select
|
NP_005620.1:p.Val422Gly
|
|
NM_001142805.2:c.1235T>G
|
NP_001136277.1:p.Val412Gly
|
|