ENST00000255078.8:c.1791C>G
MANE Select
|
ENSP00000255078.4:p.Ile597Met
|
|
ENST00000674675.1:c.35C>G
|
|
|
ENST00000674878.1:c.35C>G
|
|
|
ENST00000674955.1:c.*508C>G
|
ENSP00000502463.1:n.*508C>G
|
|
ENST00000675118.1:c.1279C>G
|
|
|
ENST00000675389.1:n.66C>G
|
|
|
ENST00000675615.1:c.1791C>G
|
ENSP00000502413.1:p.Ile597Met
|
|
ENST00000675648.1:n.1166C>G
|
|
|
ENST00000675916.1:c.35C>G
|
|
|
ENST00000676173.1:n.2536C>G
|
|
|
ENST00000676182.1:c.222C>G
|
|
|
ENST00000676228.1:c.*1114C>G
|
ENSP00000502375.1:n.*1114C>G
|
|
ENST00000255078.7:c.1791C>G
|
ENSP00000255078.3:p.Ile597Met
|
|
ENST00000539064.5:n.1550C>G
|
|
|
ENST00000541229.5:n.486C>G
|
|
|
ENST00000543739.5:n.784C>G
|
|
|
ENST00000545475.1:n.387C>G
|
|
|
NM_002180.2:c.1791C>G , LRG_250t1:c.1791C>G
|
NP_002171.2:p.Ile597Met
|
|
XM_005273974.2:c.780C>G
|
XP_005274031.1:p.Ile260Met
|
|
XM_005273975.2:c.663C>G
|
XP_005274032.1:p.Ile221Met
|
|
XM_011544994.1:c.558C>G
|
XP_011543296.1:p.Ile186Met
|
|
XR_949903.1:n.1893C>G
|
|
|
XM_005273975.3:c.663C>G
|
XP_005274032.1:p.Ile221Met
|
|
XM_017017669.2:c.780C>G
|
XP_016873158.1:p.Ile260Met
|
|
XM_017017670.2:c.780C>G
|
XP_016873159.1:p.Ile260Met
|
|
XR_949903.3:n.1889C>G
|
|
|
NM_002180.3:c.1791C>G
MANE Select
|
NP_002171.2:p.Ile597Met
|
|