ENST00000265104.5:c.8158C>T
MANE Select
|
ENSP00000265104.4:p.Leu2720Phe
|
|
ENST00000681290.1:c.8113C>T
|
ENSP00000505288.1:p.Leu2705Phe
|
|
ENST00000265104.4:c.8158C>T
|
ENSP00000265104.4:p.Leu2720Phe
|
|
NM_001369.2:c.8158C>T
|
NP_001360.1:p.Leu2720Phe
|
|
XM_005248262.2:c.8113C>T
|
XP_005248319.1:p.Leu2705Phe
|
|
XM_011513990.1:c.8158C>T
|
XP_011512292.1:p.Leu2720Phe
|
|
XR_925598.1:n.8365C>T
|
|
|
XM_005248262.3:c.8266C>T
|
XP_005248319.2:p.Leu2756Phe
|
|
XM_017009177.1:c.8266C>T
|
XP_016864666.1:p.Leu2756Phe
|
|
XM_017009178.1:c.7171C>T
|
XP_016864667.1:p.Leu2391Phe
|
|
XM_017009179.2:c.7171C>T
|
XP_016864668.1:p.Leu2391Phe
|
|
XM_017009180.1:c.8266C>T
|
XP_016864669.1:p.Leu2756Phe
|
|
XM_017009181.1:c.8266C>T
|
XP_016864670.1:p.Leu2756Phe
|
|
XM_017009182.1:c.8266C>T
|
XP_016864671.1:p.Leu2756Phe
|
|
XM_017009183.1:c.8266C>T
|
XP_016864672.1:p.Leu2756Phe
|
|
XM_017009184.1:c.8266C>T
|
XP_016864673.1:p.Leu2756Phe
|
|
XM_017009185.1:c.3355C>T
|
XP_016864674.1:p.Leu1119Phe
|
|
XM_017009186.1:c.2908C>T
|
XP_016864675.1:p.Leu970Phe
|
|
XM_017009188.1:c.2245C>T
|
XP_016864677.1:p.Leu749Phe
|
|
XM_024454388.1:c.7171C>T
|
XP_024310156.1:p.Leu2391Phe
|
|
XM_024454389.1:c.6760C>T
|
XP_024310157.1:p.Leu2254Phe
|
|
XR_001742034.1:n.8283C>T
|
|
|
XR_001742035.1:n.8283C>T
|
|
|
NM_001369.3:c.8158C>T
MANE Select
|
NP_001360.1:p.Leu2720Phe
|
|