ENST00000261292.9:c.1228T>G
MANE Select
|
ENSP00000261292.4:p.Leu410Val
|
|
ENST00000261292.8:c.1228T>G
|
ENSP00000261292.4:p.Leu410Val
|
|
ENST00000427224.6:c.1006T>G
|
ENSP00000387978.2:p.Leu336Val
|
|
NM_001308006.1:c.1006T>G
|
NP_001294935.1:p.Leu336Val
|
|
NM_006033.2:c.1228T>G
|
NP_006024.1:p.Leu410Val
|
|
NM_006033.3:c.1228T>G
|
NP_006024.1:p.Leu410Val
|
|
XM_005258390.1:c.1336T>G
|
XP_005258447.1:p.Leu446Val
|
|
XM_011526265.1:c.1114T>G
|
XP_011524567.1:p.Leu372Val
|
|
XM_011526267.1:c.988T>G
|
XP_011524569.1:p.Leu330Val
|
|
XM_011526265.3:c.1114T>G
|
XP_011524567.1:p.Leu372Val
|
|
XM_017026095.1:c.637T>G
|
XP_016881584.1:p.Leu213Val
|
|
NM_006033.4:c.1228T>G
MANE Select
|
NP_006024.1:p.Leu410Val
|
|
NM_001308006.2:c.1006T>G
|
NP_001294935.1:p.Leu336Val
|
|