ENST00000367698.4:c.1378A>C
MANE Select
|
ENSP00000356671.3:p.Asn460His
|
|
ENST00000367698.3:c.1378A>C
|
ENSP00000356671.3:p.Asn460His
|
|
ENST00000617423.4:c.763A>C
|
ENSP00000478688.1:p.Asn255His
|
|
NM_000488.3:c.1378A>C , LRG_577t1:c.1378A>C
|
NP_000479.1:p.Asn460His
|
|
XM_005245198.2:c.1234A>C
|
XP_005245255.1:p.Asn412His
|
|
NM_001365052.1:c.1234A>C
|
NP_001351981.1:p.Asn412His
|
|
NM_000488.4:c.1378A>C
MANE Select
|
NP_000479.1:p.Asn460His
|
|
NM_001365052.2:c.1234A>C
|
NP_001351981.1:p.Asn412His
|
|
NM_001386302.1:c.1501A>C
|
NP_001373231.1:p.Asn501His
|
|
NM_001386303.1:c.1459A>C
|
NP_001373232.1:p.Asn487His
|
|
NM_001386304.1:c.1357A>C
|
NP_001373233.1:p.Asn453His
|
|
NM_001386305.1:c.1321A>C
|
NP_001373234.1:p.Asn441His
|
|
NM_001386306.1:c.1162A>C
|
NP_001373235.1:p.Asn388His
|
|