ENST00000311907.10:c.756C>A
MANE Select
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ENSP00000308541.5:p.Asn252Lys
|
|
ENST00000311907.9:c.756C>A
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ENSP00000308541.5:p.Asn252Lys
|
|
ENST00000442468.1:c.726C>A
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ENSP00000387413.1:p.Asn242Lys
|
|
ENST00000490274.1:n.536C>A
|
|
|
ENST00000530231.5:c.756C>A
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ENSP00000433907.1:p.Asn252Lys
|
|
NM_000506.3:c.756C>A
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NP_000497.1:p.Asn252Lys
|
|
NM_000506.4:c.756C>A , LRG_551t1:c.756C>A
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NP_000497.1:p.Asn252Lys
|
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NM_001311257.1:c.708C>A
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NP_001298186.1:p.Asn236Lys
|
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XR_428840.2:n.800C>A
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|
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XR_428840.4:n.791C>A
|
|
|
NM_000506.5:c.756C>A
MANE Select
|
NP_000497.1:p.Asn252Lys
|
|
NM_001311257.2:c.708C>A
|
NP_001298186.1:p.Asn236Lys
|
|