ENST00000265104.5:c.12518T>G
MANE Select
|
ENSP00000265104.4:p.Leu4173Arg
|
|
ENST00000681290.1:c.12473T>G
|
ENSP00000505288.1:p.Leu4158Arg
|
|
ENST00000265104.4:c.12518T>G
|
ENSP00000265104.4:p.Leu4173Arg
|
|
NM_001369.2:c.12518T>G
|
NP_001360.1:p.Leu4173Arg
|
|
XM_005248262.2:c.12473T>G
|
XP_005248319.1:p.Leu4158Arg
|
|
XM_005248262.3:c.12626T>G
|
XP_005248319.2:p.Leu4209Arg
|
|
XM_017009177.1:c.12626T>G
|
XP_016864666.1:p.Leu4209Arg
|
|
XM_017009178.1:c.11531T>G
|
XP_016864667.1:p.Leu3844Arg
|
|
XM_017009179.2:c.11531T>G
|
XP_016864668.1:p.Leu3844Arg
|
|
XM_017009180.1:c.12626T>G
|
XP_016864669.1:p.Leu4209Arg
|
|
XM_017009185.1:c.7715T>G
|
XP_016864674.1:p.Leu2572Arg
|
|
XM_017009186.1:c.7268T>G
|
XP_016864675.1:p.Leu2423Arg
|
|
XM_017009188.1:c.6605T>G
|
XP_016864677.1:p.Leu2202Arg
|
|
XM_024454388.1:c.11531T>G
|
XP_024310156.1:p.Leu3844Arg
|
|
XM_024454389.1:c.11120T>G
|
XP_024310157.1:p.Leu3707Arg
|
|
NM_001369.3:c.12518T>G
MANE Select
|
NP_001360.1:p.Leu4173Arg
|
|