|
NM_001278055.1:c.9476T>A
|
NP_001264984.1:p.Leu3159His
|
|
|
NM_014363.5:c.9917T>A
|
NP_055178.3:p.Leu3306His
|
|
|
XM_005266338.1:c.9944T>A
|
XP_005266395.1:p.Leu3315His
|
|
|
XM_011535038.1:c.9968T>A
|
XP_011533340.1:p.Leu3323His
|
|
|
XM_011535039.1:c.9935T>A
|
XP_011533341.1:p.Leu3312His
|
|
|
XM_005266338.2:c.9944T>A
|
XP_005266395.1:p.Leu3315His
|
|
|
XM_011535039.2:c.9935T>A
|
XP_011533341.1:p.Leu3312His
|
|
|
XM_017020539.1:c.9908T>A
|
XP_016876028.1:p.Leu3303His
|
|
|
XM_024449337.1:c.9944T>A
|
XP_024305105.1:p.Leu3315His
|
|
|
NM_014363.6:c.9917T>A
MANE Select
|
NP_055178.3:p.Leu3306His
|
|
|
NM_001278055.2:c.9476T>A
|
NP_001264984.1:p.Leu3159His
|
|
|
ENST00000382292.7:c.9917T>A
|
ENSP00000371729.3:p.Leu3306His
|
|
|
ENST00000382298.7:c.9917T>A
|
ENSP00000371735.3:p.Leu3306His
|
|
|
ENST00000402364.1:c.7667T>A
|
ENSP00000385844.1:p.Leu2556His
|
|
|
ENST00000423156.1:n.1058-4475T>A
|
ENSP00000390925.1:p.=
|
|
|
ENST00000455470.5:n.2130-4475T>A
|
|
|
