ENST00000286657.10:c.1717T>G
MANE Select
|
ENSP00000286657.4:p.Phe573Val
|
|
ENST00000286657.8:c.1717T>G
|
ENSP00000286657.4:p.Phe573Val
|
|
ENST00000622135.1:c.1717T>G
|
ENSP00000480055.1:p.Phe573Val
|
|
NM_014243.2:c.1717T>G
|
NP_055058.2:p.Phe573Val
|
|
XM_011532421.1:c.1660T>G
|
XP_011530723.1:p.Phe554Val
|
|
XM_011532422.1:c.1633T>G
|
XP_011530724.1:p.Phe545Val
|
|
XM_011532423.1:c.1075T>G
|
XP_011530725.1:p.Phe359Val
|
|
XM_011532424.1:c.985T>G
|
XP_011530726.1:p.Phe329Val
|
|
XM_011532421.2:c.1660T>G
|
XP_011530723.1:p.Phe554Val
|
|
XM_011532422.3:c.1633T>G
|
XP_011530724.1:p.Phe545Val
|
|
NM_014243.3:c.1717T>G
MANE Select
|
NP_055058.2:p.Phe573Val
|
|