ENST00000286657.10:c.1678T>G
MANE Select
|
ENSP00000286657.4:p.Phe560Val
|
|
ENST00000286657.8:c.1678T>G
|
ENSP00000286657.4:p.Phe560Val
|
|
ENST00000622135.1:c.1678T>G
|
ENSP00000480055.1:p.Phe560Val
|
|
NM_014243.2:c.1678T>G
|
NP_055058.2:p.Phe560Val
|
|
XM_011532421.1:c.1621T>G
|
XP_011530723.1:p.Phe541Val
|
|
XM_011532422.1:c.1594T>G
|
XP_011530724.1:p.Phe532Val
|
|
XM_011532423.1:c.1036T>G
|
XP_011530725.1:p.Phe346Val
|
|
XM_011532424.1:c.946T>G
|
XP_011530726.1:p.Phe316Val
|
|
XM_011532421.2:c.1621T>G
|
XP_011530723.1:p.Phe541Val
|
|
XM_011532422.3:c.1594T>G
|
XP_011530724.1:p.Phe532Val
|
|
NM_014243.3:c.1678T>G
MANE Select
|
NP_055058.2:p.Phe560Val
|
|