ENST00000370086.8:c.361A>C
MANE Select
|
ENSP00000359103.3:p.Asn121His
|
|
ENST00000320857.7:c.361A>C
|
ENSP00000317331.3:p.Asn121His
|
|
ENST00000370085.3:c.286A>C
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ENSP00000359102.3:p.Asn96His
|
|
ENST00000370086.7:c.361A>C
|
ENSP00000359103.3:p.Asn121His
|
|
ENST00000370087.5:c.361A>C
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ENSP00000359104.1:p.Asn121His
|
|
ENST00000447375.1:n.201A>C
|
|
|
ENST00000460616.5:n.2069A>C
|
|
|
ENST00000471880.5:n.564A>C
|
|
|
ENST00000482902.5:n.2188A>C
|
|
|
ENST00000485612.5:n.476A>C
|
|
|
ENST00000486204.5:n.433A>C
|
|
|
NM_001204526.1:c.394A>C
|
NP_001191455.1:p.Asn132His
|
|
NM_001204527.1:c.385A>C
|
NP_001191456.1:p.Asn129His
|
|
NM_006280.2:c.361A>C
|
NP_006271.1:p.Asn121His
|
|
NR_037927.1:n.706A>C
|
|
|
XM_011531186.1:c.361A>C
|
XP_011529488.1:p.Asn121His
|
|
XM_011531187.1:c.361A>C
|
XP_011529489.1:p.Asn121His
|
|
XM_017029756.1:c.172A>C
|
XP_016885245.1:p.Asn58His
|
|
XM_017029757.1:c.172A>C
|
XP_016885246.1:p.Asn58His
|
|
XM_024452428.1:c.172A>C
|
XP_024308196.1:p.Asn58His
|
|
NM_001204527.2:c.385A>C
|
NP_001191456.1:p.Asn129His
|
|
NM_006280.3:c.361A>C
MANE Select
|
NP_006271.1:p.Asn121His
|
|