ENST00000272602.7:c.556C>T
MANE Select
|
ENSP00000272602.2:p.Leu186Phe
|
|
ENST00000272602.6:c.556C>T
|
ENSP00000272602.2:p.Leu186Phe
|
|
ENST00000393503.2:n.561C>T
|
|
|
ENST00000393504.5:c.556C>T
|
ENSP00000377140.1:p.Leu186Phe
|
|
ENST00000409937.1:c.568C>T
|
ENSP00000386761.1:p.Leu190Phe
|
|
ENST00000436404.6:c.502C>T
|
ENSP00000410070.2:p.Leu168Phe
|
|
NM_001079878.1:c.502C>T
|
NP_001073347.1:p.Leu168Phe
|
|
NM_001298.2:c.556C>T
|
NP_001289.1:p.Leu186Phe
|
|
XM_006712243.2:c.667C>T
|
XP_006712306.1:p.Leu223Phe
|
|
XM_011510554.1:c.721C>T
|
XP_011508856.1:p.Leu241Phe
|
|
XM_011510554.2:c.721C>T
|
XP_011508856.1:p.Leu241Phe
|
|
NM_001079878.2:c.502C>T
|
NP_001073347.1:p.Leu168Phe
|
|
NM_001298.3:c.556C>T
MANE Select
|
NP_001289.1:p.Leu186Phe
|
|