ENST00000584880.6:c.*398A>G
|
ENSP00000464347.2:n.*398A>G
|
|
ENST00000703608.1:c.*718A>G
|
ENSP00000515392.1:n.*718A>G
|
|
ENST00000703609.1:c.1120A>G
|
ENSP00000515393.1:p.Ile374Val
|
|
ENST00000703610.1:c.*478A>G
|
ENSP00000515394.1:n.*478A>G
|
|
ENST00000310144.11:c.1201A>G
MANE Select
|
ENSP00000310572.6:p.Ile401Val
|
|
ENST00000310144.10:c.1201A>G
|
ENSP00000310572.6:p.Ile401Val
|
|
ENST00000375812.8:c.1177A>G
|
ENSP00000364970.4:p.Ile393Val
|
|
ENST00000578570.5:n.1611A>G
|
|
|
ENST00000579147.5:n.2516A>G
|
|
|
ENST00000580864.5:c.1177A>G
|
ENSP00000462495.1:p.Ile393Val
|
|
ENST00000581882.5:c.1177A>G
|
ENSP00000463938.1:p.Ile393Val
|
|
ENST00000584657.1:n.506A>G
|
|
|
ENST00000585242.5:c.*972A>G
|
ENSP00000463107.1:n.*972A>G
|
|
NM_001199163.1:c.1177A>G
|
NP_001186092.1:p.Ile393Val
|
|
NM_002805.5:c.1201A>G
|
NP_002796.4:p.Ile401Val
|
|
XM_006721980.1:c.1201A>G
|
XP_006722043.1:p.Ile401Val
|
|
XR_934508.1:n.1290A>G
|
|
|
XM_024450840.1:c.1282A>G
|
XP_024306608.1:p.Ile428Val
|
|
XM_024450841.1:c.1258A>G
|
XP_024306609.1:p.Ile420Val
|
|
XR_934508.2:n.1277A>G
|
|
|
NM_002805.6:c.1201A>G
MANE Select
|
NP_002796.4:p.Ile401Val
|
|
NM_001199163.2:c.1177A>G
|
NP_001186092.1:p.Ile393Val
|
|