ENST00000267845.8:c.1693C>G
MANE Select
|
ENSP00000267845.3:p.Leu565Val
|
|
ENST00000267845.7:c.1693C>G
|
ENSP00000267845.3:p.Leu565Val
|
|
ENST00000543581.5:c.1594C>G
|
ENSP00000440252.1:p.Leu532Val
|
|
ENST00000559816.1:n.1437C>G
|
|
|
NM_001306146.1:c.1594C>G
|
NP_001293075.1:p.Leu532Val
|
|
NM_002112.3:c.1693C>G
|
NP_002103.2:p.Leu565Val
|
|
XM_011521479.1:c.1456C>G
|
XP_011519781.1:p.Leu486Val
|
|
XM_011521480.1:c.1261C>G
|
XP_011519782.1:p.Leu421Val
|
|
XM_017022094.1:c.1798C>G
|
XP_016877583.1:p.Leu600Val
|
|
XM_017022095.1:c.1699C>G
|
XP_016877584.1:p.Leu567Val
|
|
XM_017022096.1:c.1570C>G
|
XP_016877585.1:p.Leu524Val
|
|
XM_017022097.1:c.1561C>G
|
XP_016877586.1:p.Leu521Val
|
|
XM_017022098.1:c.1366C>G
|
XP_016877587.1:p.Leu456Val
|
|
NM_002112.4:c.1693C>G
MANE Select
|
NP_002103.2:p.Leu565Val
|
|
NM_001306146.2:c.1594C>G
|
NP_001293075.1:p.Leu532Val
|
|