ENST00000403733.8:c.3372A>C
MANE Select
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ENSP00000384222.3:p.Gln1124His
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ENST00000403733.7:c.3372A>C
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ENSP00000384222.3:p.Gln1124His
|
|
ENST00000427431.5:c.*2764A>C
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ENSP00000393342.1:n.*2764A>C
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ENST00000438543.5:c.*1168A>C
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ENSP00000413521.1:n.*1168A>C
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ENST00000448232.6:c.3444A>C
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ENSP00000398577.2:p.Gln1148His
|
|
ENST00000504005.5:c.2418A>C
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ENSP00000427569.1:p.Gln806His
|
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ENST00000508747.1:c.756A>C
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ENSP00000420835.1:p.Gln252His
|
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ENST00000513834.5:c.3225A>C
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ENSP00000425054.1:p.Gln1075His
|
|
NM_024949.5:c.3372A>C
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NP_079225.5:p.Gln1124His
|
|
XM_011532269.1:c.3444A>C
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XP_011530571.1:p.Gln1148His
|
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XM_011532269.3:c.3444A>C
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XP_011530571.1:p.Gln1148His
|
|
XM_024454225.1:c.3150A>C
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XP_024309993.1:p.Gln1050His
|
|
NM_024949.6:c.3372A>C
MANE Select
|
NP_079225.5:p.Gln1124His
|
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