ENST00000389857.11:c.5114A>C
MANE Select
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ENSP00000374507.6:p.Asp1705Ala
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ENST00000331194.8:c.686A>C
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ENSP00000330332.8:p.Asp229Ala
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ENST00000334448.5:n.926A>C
|
|
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ENST00000389857.10:c.5114A>C
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ENSP00000374507.6:p.Asp1705Ala
|
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ENST00000556726.5:c.1342A>C
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NM_001080414.3:c.5114A>C
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NP_001073883.2:p.Asp1705Ala
|
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XM_011536796.1:c.5006A>C
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XP_011535098.1:p.Asp1669Ala
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XR_429316.2:n.5389A>C
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XM_011536796.2:c.5006A>C
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XP_011535098.1:p.Asp1669Ala
|
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XM_017021336.1:c.2195A>C
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XP_016876825.1:p.Asp732Ala
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XR_429316.4:n.5387A>C
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|
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NM_001080414.4:c.5114A>C
MANE Select
|
NP_001073883.2:p.Asp1705Ala
|
|