ENST00000452035.7:n.2142A>C
|
|
|
ENST00000483004.2:c.1534A>C
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ENSP00000419887.2:p.Asn512His
|
|
ENST00000698628.1:c.1624+341A>C
|
ENSP00000513848.1:n.1624+341A>C
|
|
ENST00000698629.1:n.1927A>C
|
|
|
ENST00000698630.1:n.2466A>C
|
|
|
ENST00000698631.1:n.2467A>C
|
|
|
ENST00000698632.1:n.3261A>C
|
|
|
ENST00000698633.1:n.3151A>C
|
|
|
ENST00000698636.1:n.1972A>C
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|
|
ENST00000425368.7:c.1750A>C
MANE Select
|
ENSP00000416561.2:p.Asn584His
|
|
ENST00000425368.6:c.1750A>C
|
ENSP00000416561.2:p.Asn584His
|
|
ENST00000456570.5:c.3256A>C
|
ENSP00000410815.1:p.Asn1086His
|
|
ENST00000467360.1:n.876A>C
|
|
|
ENST00000477310.1:c.2803A>C
|
ENSP00000418996.1:p.Asn935His
|
|
ENST00000483004.1:c.372A>C
|
|
|
NM_001710.5:c.1750A>C , LRG_136t1:c.1750A>C
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NP_001701.2:p.Asn584His
|
|
NM_001710.6:c.1750A>C
MANE Select
|
NP_001701.2:p.Asn584His
|
|