ENST00000367698.4:c.1345C>G
MANE Select
|
ENSP00000356671.3:p.Leu449Val
|
|
ENST00000367698.3:c.1345C>G
|
ENSP00000356671.3:p.Leu449Val
|
|
ENST00000617423.4:c.730C>G
|
ENSP00000478688.1:p.Leu244Val
|
|
NM_000488.3:c.1345C>G , LRG_577t1:c.1345C>G
|
NP_000479.1:p.Leu449Val
|
|
XM_005245198.2:c.1201C>G
|
XP_005245255.1:p.Leu401Val
|
|
NM_001365052.1:c.1201C>G
|
NP_001351981.1:p.Leu401Val
|
|
NM_000488.4:c.1345C>G
MANE Select
|
NP_000479.1:p.Leu449Val
|
|
NM_001365052.2:c.1201C>G
|
NP_001351981.1:p.Leu401Val
|
|
NM_001386302.1:c.1468C>G
|
NP_001373231.1:p.Leu490Val
|
|
NM_001386303.1:c.1426C>G
|
NP_001373232.1:p.Leu476Val
|
|
NM_001386304.1:c.1324C>G
|
NP_001373233.1:p.Leu442Val
|
|
NM_001386305.1:c.1288C>G
|
NP_001373234.1:p.Leu430Val
|
|
NM_001386306.1:c.1129C>G
|
NP_001373235.1:p.Leu377Val
|
|