ENST00000399408.7:c.4042C>G
|
ENSP00000382340.4:p.Leu1348Val
|
|
ENST00000399410.8:c.4012C>G
MANE Select
|
ENSP00000382342.3:p.Leu1338Val
|
|
ENST00000572882.3:c.3835C>G
|
ENSP00000461615.2:p.Leu1279Val
|
|
ENST00000676806.1:n.738C>G
|
|
|
ENST00000677164.1:c.3541C>G
|
ENSP00000502873.1:p.Leu1181Val
|
|
ENST00000678422.1:c.*1304C>G
|
ENSP00000503954.1:n.*1304C>G
|
|
ENST00000399408.6:c.3064C>G
|
ENSP00000382340.3:p.Leu1022Val
|
|
ENST00000399410.7:c.4012C>G
|
ENSP00000382342.3:p.Leu1338Val
|
|
ENST00000572882.2:c.3737C>G
|
|
|
NM_004996.3:c.4012C>G
|
NP_004987.2:p.Leu1338Val
|
|
XM_011522497.1:c.3988C>G
|
XP_011520799.1:p.Leu1330Val
|
|
XM_011522498.1:c.3919C>G
|
XP_011520800.1:p.Leu1307Val
|
|
XM_011522498.2:c.3919C>G
|
XP_011520800.1:p.Leu1307Val
|
|
XM_017023237.1:c.4066C>G
|
XP_016878726.1:p.Leu1356Val
|
|
XM_017023238.1:c.3940C>G
|
XP_016878727.1:p.Leu1314Val
|
|
XM_017023239.1:c.3928C>G
|
XP_016878728.1:p.Leu1310Val
|
|
XM_017023240.1:c.3889C>G
|
XP_016878729.1:p.Leu1297Val
|
|
XM_017023241.1:c.3802C>G
|
XP_016878730.1:p.Leu1268Val
|
|
XM_017023242.1:c.3721C>G
|
XP_016878731.1:p.Leu1241Val
|
|
NM_004996.4:c.4012C>G
MANE Select
|
NP_004987.2:p.Leu1338Val
|
|