ENST00000696982.1:c.1091C>T
|
ENSP00000513017.1:p.Ala364Val
|
|
ENST00000527786.7:c.1070C>T
MANE Select
|
ENSP00000433488.2:p.Ala357Val
|
|
ENST00000281428.12:c.872C>T
|
ENSP00000281428.8:p.Ala291Val
|
|
ENST00000344954.10:c.491C>T
|
ENSP00000339627.7:p.Ala164Val
|
|
ENST00000429175.7:c.*992C>T
|
ENSP00000399985.3:n.*992C>T
|
|
ENST00000527786.6:c.1070C>T
|
ENSP00000433488.2:p.Ala357Val
|
|
ENST00000528790.1:n.3653C>T
|
|
|
ENST00000534087.3:c.971C>T
|
ENSP00000432950.1:p.Ala324Val
|
|
ENST00000608303.5:c.*462C>T
|
ENSP00000477262.1:n.*462C>T
|
|
NM_001167681.2:c.971C>T
|
NP_001161153.1:p.Ala324Val
|
|
NM_001271010.1:c.872C>T
|
NP_001257939.1:p.Ala291Val
|
|
NM_001271012.1:c.491C>T
|
NP_001257941.1:p.Ala164Val
|
|
NM_002017.4:c.1070C>T
|
NP_002008.2:p.Ala357Val
|
|
XM_011542701.1:c.971C>T
|
XP_011541003.1:p.Ala324Val
|
|
XM_011542702.1:c.944C>T
|
XP_011541004.1:p.Ala315Val
|
|
XM_011542701.2:c.971C>T
|
XP_011541003.1:p.Ala324Val
|
|
XM_017017405.1:c.971C>T
|
XP_016872894.1:p.Ala324Val
|
|
XM_017017406.1:c.971C>T
|
XP_016872895.1:p.Ala324Val
|
|
NM_002017.5:c.1070C>T
MANE Select
|
NP_002008.2:p.Ala357Val
|
|
NM_001167681.3:c.971C>T
|
NP_001161153.1:p.Ala324Val
|
|
NM_001271010.2:c.872C>T
|
NP_001257939.1:p.Ala291Val
|
|
NM_001271012.2:c.491C>T
|
NP_001257941.1:p.Ala164Val
|
|