ENST00000389048.8:c.3505C>G
MANE Select
|
ENSP00000373700.3:p.Leu1169Val
|
|
ENST00000431873.6:c.732C>G
|
|
|
ENST00000638605.1:n.382C>G
|
|
|
ENST00000642122.1:c.301C>G
|
ENSP00000493203.1:p.Leu101Val
|
|
ENST00000389048.7:c.3505C>G
|
ENSP00000373700.3:p.Leu1169Val
|
|
ENST00000431873.5:c.385C>G
|
ENSP00000414027.2:p.Leu129Val
|
|
ENST00000453137.1:c.199C>G
|
ENSP00000387488.1:p.Leu67Val
|
|
ENST00000618119.4:c.2374C>G
|
ENSP00000482733.1:p.Leu792Val
|
|
NM_004304.4:c.3505C>G
|
NP_004295.2:p.Leu1169Val
|
|
NM_001353765.1:c.301C>G
|
NP_001340694.1:p.Leu101Val
|
|
XM_024452778.1:c.658C>G
|
XP_024308546.1:p.Leu220Val
|
|
XM_024452779.1:c.301C>G
|
XP_024308547.1:p.Leu101Val
|
|
NM_004304.5:c.3505C>G
MANE Select
|
NP_004295.2:p.Leu1169Val
|
|
NM_001353765.2:c.301C>G
|
NP_001340694.1:p.Leu101Val
|
|