ENST00000265104.5:c.8395C>G
MANE Select
|
ENSP00000265104.4:p.Arg2799Gly
|
|
ENST00000681290.1:c.8350C>G
|
ENSP00000505288.1:p.Arg2784Gly
|
|
ENST00000265104.4:c.8395C>G
|
ENSP00000265104.4:p.Arg2799Gly
|
|
NM_001369.2:c.8395C>G
|
NP_001360.1:p.Arg2799Gly
|
|
XM_005248262.2:c.8350C>G
|
XP_005248319.1:p.Arg2784Gly
|
|
XM_011513990.1:c.8395C>G
|
XP_011512292.1:p.Arg2799Gly
|
|
XR_925598.1:n.8602C>G
|
|
|
XM_005248262.3:c.8503C>G
|
XP_005248319.2:p.Arg2835Gly
|
|
XM_017009177.1:c.8503C>G
|
XP_016864666.1:p.Arg2835Gly
|
|
XM_017009178.1:c.7408C>G
|
XP_016864667.1:p.Arg2470Gly
|
|
XM_017009179.2:c.7408C>G
|
XP_016864668.1:p.Arg2470Gly
|
|
XM_017009180.1:c.8503C>G
|
XP_016864669.1:p.Arg2835Gly
|
|
XM_017009181.1:c.8503C>G
|
XP_016864670.1:p.Arg2835Gly
|
|
XM_017009182.1:c.8503C>G
|
XP_016864671.1:p.Arg2835Gly
|
|
XM_017009183.1:c.8503C>G
|
XP_016864672.1:p.Arg2835Gly
|
|
XM_017009184.1:c.8503C>G
|
XP_016864673.1:p.Arg2835Gly
|
|
XM_017009185.1:c.3592C>G
|
XP_016864674.1:p.Arg1198Gly
|
|
XM_017009186.1:c.3145C>G
|
XP_016864675.1:p.Arg1049Gly
|
|
XM_017009188.1:c.2482C>G
|
XP_016864677.1:p.Arg828Gly
|
|
XM_024454388.1:c.7408C>G
|
XP_024310156.1:p.Arg2470Gly
|
|
XM_024454389.1:c.6997C>G
|
XP_024310157.1:p.Arg2333Gly
|
|
XR_001742034.1:n.8520C>G
|
|
|
XR_001742035.1:n.8520C>G
|
|
|
NM_001369.3:c.8395C>G
MANE Select
|
NP_001360.1:p.Arg2799Gly
|
|