ENST00000315757.9:c.1291T>G
MANE Select
|
ENSP00000327290.7:p.Ser431Ala
|
|
ENST00000315757.8:c.1291T>G
|
ENSP00000327290.7:p.Ser431Ala
|
|
ENST00000423218.6:c.1291T>G
|
ENSP00000403392.2:p.Ser431Ala
|
|
ENST00000566429.1:n.197-17T>G
|
|
|
ENST00000569346.5:n.270T>G
|
|
|
NM_001004439.1:c.1291T>G
|
NP_001004439.1:p.Ser431Ala
|
|
XM_005254228.2:c.985T>G
|
XP_005254285.1:p.Ser329Ala
|
|
XM_011521363.1:c.1084T>G
|
XP_011519665.1:p.Ser362Ala
|
|
XM_005254228.3:c.985T>G
|
XP_005254285.1:p.Ser329Ala
|
|
XM_011521363.2:c.1084T>G
|
XP_011519665.1:p.Ser362Ala
|
|
NM_001004439.2:c.1291T>G
MANE Select
|
NP_001004439.1:p.Ser431Ala
|
|