ENST00000647814.1:c.2703A>G
MANE Select
|
ENSP00000497274.1:p.Ile901Met
|
|
ENST00000370449.8:c.2703A>G
|
ENSP00000359478.4:p.Ile901Met
|
|
NM_000392.4:c.2703A>G
|
NP_000383.1:p.Ile901Met
|
|
XM_006717630.2:c.2007A>G
|
XP_006717693.1:p.Ile669Met
|
|
XM_006717631.2:c.*130A>G
|
XP_006717694.1:n.*130A>G
|
|
XM_011539291.1:c.2703A>G
|
XP_011537593.1:p.Ile901Met
|
|
XR_945604.1:n.2892A>G
|
|
|
XR_945605.1:n.2894A>G
|
|
|
NM_000392.5:c.2703A>G
MANE Select
|
NP_000383.2:p.Ile901Met
|
|
XM_006717630.3:c.2007A>G
|
XP_006717693.1:p.Ile669Met
|
|
XM_006717631.4:c.*130A>G
|
XP_006717694.1:n.*130A>G
|
|
XM_011539291.3:c.2703A>G
|
XP_011537593.1:p.Ile901Met
|
|
XR_945604.3:n.2946A>G
|
|
|
XR_945605.3:n.2946A>G
|
|
|