ENST00000367698.4:c.1322T>G
MANE Select
|
ENSP00000356671.3:p.Leu441Arg
|
|
ENST00000367698.3:c.1322T>G
|
ENSP00000356671.3:p.Leu441Arg
|
|
ENST00000617423.4:c.707T>G
|
ENSP00000478688.1:p.Leu236Arg
|
|
NM_000488.3:c.1322T>G , LRG_577t1:c.1322T>G
|
NP_000479.1:p.Leu441Arg
|
|
XM_005245198.2:c.1178T>G
|
XP_005245255.1:p.Leu393Arg
|
|
NM_001365052.1:c.1178T>G
|
NP_001351981.1:p.Leu393Arg
|
|
NM_000488.4:c.1322T>G
MANE Select
|
NP_000479.1:p.Leu441Arg
|
|
NM_001365052.2:c.1178T>G
|
NP_001351981.1:p.Leu393Arg
|
|
NM_001386302.1:c.1445T>G
|
NP_001373231.1:p.Leu482Arg
|
|
NM_001386303.1:c.1403T>G
|
NP_001373232.1:p.Leu468Arg
|
|
NM_001386304.1:c.1301T>G
|
NP_001373233.1:p.Leu434Arg
|
|
NM_001386305.1:c.1265T>G
|
NP_001373234.1:p.Leu422Arg
|
|
NM_001386306.1:c.1106T>G
|
NP_001373235.1:p.Leu369Arg
|
|