ENST00000265104.5:c.12612G>A
MANE Select
|
ENSP00000265104.4:p.Leu4204=
|
|
ENST00000681290.1:c.12567G>A
|
ENSP00000505288.1:p.Leu4189=
|
|
ENST00000265104.4:c.12612G>A
|
ENSP00000265104.4:p.Leu4204=
|
|
NM_001369.2:c.12612G>A
|
NP_001360.1:p.Leu4204=
|
|
XM_005248262.2:c.12567G>A
|
XP_005248319.1:p.Leu4189=
|
|
XM_005248262.3:c.12720G>A
|
XP_005248319.2:p.Leu4240=
|
|
XM_017009177.1:c.12720G>A
|
XP_016864666.1:p.Leu4240=
|
|
XM_017009178.1:c.11625G>A
|
XP_016864667.1:p.Leu3875=
|
|
XM_017009179.2:c.11625G>A
|
XP_016864668.1:p.Leu3875=
|
|
XM_017009180.1:c.12720G>A
|
XP_016864669.1:p.Leu4240=
|
|
XM_017009185.1:c.7809G>A
|
XP_016864674.1:p.Leu2603=
|
|
XM_017009186.1:c.7362G>A
|
XP_016864675.1:p.Leu2454=
|
|
XM_017009188.1:c.6699G>A
|
XP_016864677.1:p.Leu2233=
|
|
XM_024454388.1:c.11625G>A
|
XP_024310156.1:p.Leu3875=
|
|
XM_024454389.1:c.11214G>A
|
XP_024310157.1:p.Leu3738=
|
|
NM_001369.3:c.12612G>A
MANE Select
|
NP_001360.1:p.Leu4204=
|
|