ENST00000345003.9:c.514A=
MANE Select
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ENSP00000340736.4:p.Ser172=
|
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ENST00000296048.10:c.514A=
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ENSP00000296048.6:p.Ser172=
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|
ENST00000345003.8:c.514A=
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ENSP00000340736.4:p.Ser172=
|
|
ENST00000461191.1:c.502A=
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ENSP00000420247.1:p.Ser168=
|
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ENST00000469873.1:n.428A=
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|
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ENST00000479119.1:n.130A=
|
|
|
ENST00000483267.5:c.469+12416A=
|
ENSP00000419499.1:n.469+12416A=
|
|
ENST00000484197.5:c.514A=
|
ENSP00000420683.1:p.Ser172=
|
|
ENST00000497528.5:n.153A=
|
|
|
ENST00000627418.2:c.469+12416A=
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ENSP00000486061.1:n.469+12416A=
|
|
NM_001184720.1:c.514A=
|
NP_001171649.1:p.Ser172=
|
|
NM_001184721.1:c.514A=
|
NP_001171650.1:p.Ser172=
|
|
NM_004130.3:c.514A=
|
NP_004121.2:p.Ser172=
|
|
XM_017006275.1:c.337A=
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XP_016861764.1:p.Ser113=
|
|
XM_017006276.1:c.52A=
|
XP_016861765.1:p.Ser18=
|
|
NM_004130.4:c.514A=
MANE Select
|
NP_004121.2:p.Ser172=
|
|
NM_001184720.2:c.514A=
|
NP_001171649.1:p.Ser172=
|
|
NM_001184721.2:c.514A=
|
NP_001171650.1:p.Ser172=
|
|