ENST00000205402.10:c.1061G>T
MANE Select
|
ENSP00000205402.3:p.Gly354Val
|
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ENST00000205402.9:c.1061G>T
|
ENSP00000205402.3:p.Gly354Val
|
|
ENST00000415325.5:c.*735G>T
|
ENSP00000402593.1:n.*735G>T
|
|
ENST00000417551.5:c.1061G>T
|
ENSP00000390667.1:p.Gly354Val
|
|
ENST00000437604.6:c.917G>T
|
ENSP00000387542.2:p.Gly306Val
|
|
ENST00000440410.5:c.992G>T
|
ENSP00000417016.1:p.Gly331Val
|
|
NM_000108.4:c.1061G>T
|
NP_000099.2:p.Gly354Val
|
|
NM_001289750.1:c.764G>T
|
NP_001276679.1:p.Gly255Val
|
|
NM_001289751.1:c.992G>T
|
NP_001276680.1:p.Gly331Val
|
|
NM_001289752.1:c.917G>T
|
NP_001276681.1:p.Gly306Val
|
|
NM_000108.5:c.1061G>T
MANE Select
|
NP_000099.2:p.Gly354Val
|
|