ENST00000403733.8:c.3266C>T
MANE Select
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ENSP00000384222.3:p.Ala1089Val
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ENST00000403733.7:c.3266C>T
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ENSP00000384222.3:p.Ala1089Val
|
|
ENST00000427431.5:c.*2658C>T
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ENSP00000393342.1:n.*2658C>T
|
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ENST00000438543.5:c.*1062C>T
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ENSP00000413521.1:n.*1062C>T
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ENST00000448232.6:c.3338C>T
|
ENSP00000398577.2:p.Ala1113Val
|
|
ENST00000504005.5:c.2312C>T
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ENSP00000427569.1:p.Ala771Val
|
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ENST00000508747.1:c.650C>T
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ENSP00000420835.1:p.Ala217Val
|
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ENST00000513834.5:c.3119C>T
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ENSP00000425054.1:p.Ala1040Val
|
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NM_024949.5:c.3266C>T
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NP_079225.5:p.Ala1089Val
|
|
XM_011532269.1:c.3338C>T
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XP_011530571.1:p.Ala1113Val
|
|
XM_011532269.3:c.3338C>T
|
XP_011530571.1:p.Ala1113Val
|
|
XM_024454225.1:c.3044C>T
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XP_024309993.1:p.Ala1015Val
|
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NM_024949.6:c.3266C>T
MANE Select
|
NP_079225.5:p.Ala1089Val
|
|